Pattern Dystrophy Of The Retina

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Results for "Pattern Dystrophy Of The Retina": 31 genes, 1001 gene sets

Name
EEGV1 Gene electro-encephalographic variant pattern* 1*
MDRV Gene muscular dystrophy, with rimmed vacuoles
MCDR3 Gene macular dystrophy, retinal 3
MCDR1 Gene macular dystrophy, retinal, 1 (North Carolina type)
MCDR4 Gene macular dystrophy, retinal, 4 (North Carolina type with progressive sensorineural hearing loss)
CYMD Gene cystoid macular dystrophy
LGMD1H Gene limb girdle muscular dystrophy* 1H (autosomal dominant)*
LGMD1G Gene limb girdle muscular dystrophy* 1G (autosomal dominant)*
FECD7 Gene Corneal dystrophy, Fuchs endothelial, 7
FECD5 Gene Corneal dystrophy, Fuchs endothelial, 5
FECD3 Gene Corneal dystrophy, Fuchs endothelial, 3
FECD2 Gene corneal dystrophy, Fuchs endothelial 2
MDC1B Gene Muscular dystrophy, congenital, 1B
VMD1 Gene vitelliform macular dystrophy, atypical
CDB2 Gene corneal dystrophy* of Bowman layer type II (Thiel-Behnke)*
CACD Gene central areolar choroidal dystrophy
COD2 Gene cone dystrophy* 2 (X-linked)*
FSHMD1A Gene facioscapulohumeral muscular dystrophy* 1A* Facioscapulohumeral muscular dystrophy (FSHD) is a common hereditary disease of muscle. Patients with FSHD have a chromosomal rearrangement within the subtelomeric region of chromosome 4 (4q35). This region is composed mainly of a polymorphic repeat structure consisting of 3.3 kb repeat units, designated D4Z4. The number of repeat units varies from 10 to more than 100 in the population, however, in FSHD patients only 1-10 repeat units is observed because of a deletion of an integral number of these units. FSHD is caused by an epigenetic mechanism involving the contraction of a subtelomeric macrosatellite repeat, which results in marked hypomethylation of the contracted D4Z4 allele. It is likely not the structure, but the deregulation of transcription of one or more genes as a result of repeat-contraction-mediated chromatin alterations, that causes FSHD. [provided by RefSeq, Sep 2011]
FSHMD1B Gene facioscapulohumeral muscular dystrophy* 1B*
CORD8 Gene cone rod dystrophy* 8*
CORD1 Gene cone rod dystrophy* 1 (autosomal dominant)*
CORD4 Gene cone rod dystrophy* 4*
CACD3 Gene Choroidal dystrophy, central areolar 3
LECD Gene Corneal dystrophy, Lisch epithelial
MDBS2 Gene butterfly-shaped pigmentary macular dystrophy* 2*
RCD1 Gene retinal cone dystrophy 1
CORD17 Gene cone rod dystrophy* 17 (autosomal dominant)*
ATD Gene asphixiating thoracic dystrophy* (chondroectodermal dysplasia-like syndrome)*
MDCMP Gene muscular dystrophy, congenital, merosin-positive
XECD Gene Corneal dystrophy, endothelial, X-linked
CHED1 Gene corneal endothelial dystrophy* 1 (autosomal dominant)*
Pattern Dystrophy Of The Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pattern Dystrophy Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abnormal retina blood vessel pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina blood vessel pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multifocal pattern dystrophy simulating fundus flavimaculatus Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multifocal pattern dystrophy simulating fundus flavimaculatus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
becker muscular dystrophy; duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
male-pattern baldness Gene Set From GAD Gene-Disease Associations genes associated with the disease male-pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
male pattern baldness Gene Set From GAD Gene-Disease Associations genes associated with the disease male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovaries and premature male pattern baldness Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovaries and premature male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pattern Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term pattern in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
embryonic heart tube anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation involved in nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior compartment pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cytoplasmic pattern recognition receptor signaling pathway in response to virus Gene Set From GO Biological Process Annotations 2015 genes participating in the cytoplasmic pattern recognition receptor signaling pathway in response to virus biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern specification involved in kidney development Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation involved in metanephric nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior pattern specification involved in kidney development Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
lung pattern specification process Gene Set From GO Biological Process Annotations 2015 genes participating in the lung pattern specification process biological process from the curated GO Biological Process Annotations 2015 dataset.
neural plate pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the neural plate pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
cell fate commitment involved in pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the cell fate commitment involved in pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
compartment pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the compartment pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
cell fate specification involved in pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the cell fate specification involved in pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern specification involved in metanephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern specification involved in metanephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
forebrain dorsal/ventral pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the forebrain dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
radial pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the radial pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
dorsal/ventral pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern specification involved in mesonephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern specification involved in mesonephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
left/right pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the left/right pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
cell surface pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the cell surface pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern specification process Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern specification process biological process from the curated GO Biological Process Annotations 2015 dataset.
anterior/posterior pattern specification involved in ureteric bud development Gene Set From GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
forebrain anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic heart tube left/right pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern specification involved in pronephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern specification involved in pronephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cell fate determination involved in pattern specification Gene Set From GO Biological Process Annotations 2015 genes participating in the cell fate determination involved in pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset.
signaling pattern recognition receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the signaling pattern recognition receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
pattern binding Gene Set From GO Molecular Function Annotations 2015 genes performing the pattern binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
pattern recognition receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the pattern recognition receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Male-pattern baldness Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Male-pattern baldness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
termporal pattern Gene Set From GWASdb SNP-Phenotype Associations genes associated with the termporal pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
acquired abnormal hair pattern Gene Set From GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal hair pattern Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
reduced amplitude of pattern visual evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the reduced amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal branching pattern of the aortic arch Gene Set From HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital abnormal hair pattern Gene Set From HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
termporal pattern Gene Set From HPO Gene-Disease Associations genes associated with the termporal pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal hair pattern Gene Set From HPO Gene-Disease Associations genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal pattern of respiration Gene Set From HPO Gene-Disease Associations genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acquired abnormal hair pattern Gene Set From HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Pattern Recognition, Physiological Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pattern Recognition, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pattern Recognition, Visual Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pattern Recognition, Visual phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal sympathetic neuron innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mammary gland pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal non-rapid eye movement sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal urination pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal urination pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal brain wave pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal central pattern generator function Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal breathing pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal breathing pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear ihc efferent innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear ihc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sensory neuron innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal paradoxical sleep pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear ihc afferent innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear ihc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal innervation pattern to muscle Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal innervation pattern to muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal olfactory neuron innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal phrenic nerve innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal phrenic nerve innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal blood vessel pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear ohc efferent innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear ohc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal enamel rod pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal enamel rod pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal motor neuron innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal phrenic nerve innervation pattern to diaphragm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal phrenic nerve innervation pattern to diaphragm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
distorted hair follicle pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear ohc afferent innervation pattern Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear ohc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Abnormal Dermatoglyphic Pattern Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Dermatoglyphic Pattern in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Hair Pattern Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Hair Pattern in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Abnormal Hair Pattern Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Abnormal Hair Pattern in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Pattern On Pulmonary Hrct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reticular Pattern On Pulmonary Hrct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Female Pattern Alopecia (Disorder) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Pattern Alopecia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Timing Of Pattern Reversal Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Timing Of Pattern Reversal Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Pattern Of Respiration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Pattern Of Respiration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Crazy Paving Pattern On Pulmonary Hrct Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Crazy Paving Pattern On Pulmonary Hrct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Brugada Ecg Pattern Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brugada Ecg Pattern in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Amplitude Of Pattern Reversal Visual Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cytosolic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the cytosolic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
cell surface pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the cell surface pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2023 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
dorsal/ventral pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
forebrain dorsal/ventral pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the forebrain dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
embryonic heart tube anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2023 dataset.
anterior compartment pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
embryonic heart tube left/right pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
left/right pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the left/right pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
pattern specification involved in metanephros development Gene Set From GO Biological Process Annotations 2023 genes participating in the pattern specification involved in metanephros development biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of action potential firing pattern Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of action potential firing pattern biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
compartment pattern specification Gene Set From GO Biological Process Annotations 2023 genes participating in the compartment pattern specification biological process from the curated GO Biological Process Annotations 2023 dataset.
pattern specification involved in pronephros development Gene Set From GO Biological Process Annotations 2023 genes participating in the pattern specification involved in pronephros development biological process from the curated GO Biological Process Annotations 2023 dataset.
anterior/posterior pattern specification involved in kidney development Gene Set From GO Biological Process Annotations 2023 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal sensory neuron innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sensory neuron innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cochlear IHC afferent innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear IHC afferent innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal breathing pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal breathing pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mandibular nerve innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mandibular nerve innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal motor neuron innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal innervation pattern to muscle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal innervation pattern to muscle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cochlear OHC afferent innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear OHC afferent innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
distorted hair follicle pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal enamel rod pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enamel rod pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal brain wave pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cochlear OHC efferent innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear OHC efferent innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sympathetic neuron innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal central pattern generator function Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal olfactory neuron innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory neuron innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cochlear IHC efferent innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear IHC efferent innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal paradoxical sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal non-rapid eye movement sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal capillary branching pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal capillary branching pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal urination pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urination pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lacrimal gland innervation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal phrenic nerve innervation pattern to diaphragm Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal phrenic nerve innervation pattern to diaphragm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pigmentation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pigmentation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mammary gland pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
variegated eye pigmentation pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the variegated eye pigmentation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal slow-wave sleep pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal slow-wave sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal dendrite arborization pattern Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dendrite arborization pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
cell surface pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the cell surface pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2025 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
dorsal/ventral pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
forebrain dorsal/ventral pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the forebrain dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
embryonic heart tube anterior/posterior pattern specification Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2025 dataset.
anterior compartment pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
embryonic heart tube left/right pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
left/right pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the left/right pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
pattern specification involved in metanephros development Gene Set From GO Biological Process Annotations 2025 genes participating in the pattern specification involved in metanephros development biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of action potential firing pattern Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of action potential firing pattern biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of cytoplasmic pattern recognition receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
compartment pattern specification Gene Set From GO Biological Process Annotations 2025 genes participating in the compartment pattern specification biological process from the curated GO Biological Process Annotations 2025 dataset.
pattern specification involved in pronephros development Gene Set From GO Biological Process Annotations 2025 genes participating in the pattern specification involved in pronephros development biological process from the curated GO Biological Process Annotations 2025 dataset.
anterior/posterior pattern specification involved in kidney development Gene Set From GO Biological Process Annotations 2025 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
Wolff-Parkinson-White pattern Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Wolff-Parkinson-White pattern phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Male-pattern baldness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Male-pattern baldness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Local histogram emphysema pattern Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Local histogram emphysema pattern phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Western dietary pattern Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Western dietary pattern phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Prudent dietary pattern Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Prudent dietary pattern phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
retina Gene Set From BioGPS Human Cell Type and Tissue Gene Expression Profiles genes with high or low expression in retina relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
retina Gene Set From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles genes with high or low expression in retina relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
CCND1-20090754-RETINA-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CCND1-20090754-RETINA-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck retina, familial benign Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
retina lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retina lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retina Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term retina in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
SYNCRIP_OE_GDS3186_84_mouse_wild type 129 mouse retina Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SYNCRIP_OE_GDS3186_84_mouse_wild type 129 mouse retina gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
retina development in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
retina layer formation Gene Set From GO Biological Process Annotations 2015 genes participating in the retina layer formation biological process from the curated GO Biological Process Annotations 2015 dataset.
post-embryonic retina morphogenesis in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the post-embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of neural retina development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of neural retina development biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic retina morphogenesis in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
retina vasculature development in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
retina morphogenesis in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
retina homeostasis Gene Set From GO Biological Process Annotations 2015 genes participating in the retina homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of retina development in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
neural retina development Gene Set From GO Biological Process Annotations 2015 genes participating in the neural retina development biological process from the curated GO Biological Process Annotations 2015 dataset.
retina vasculature morphogenesis in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the retina vasculature morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormality of the retina Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
adult retina Gene Set From HPM Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in adult retina relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset.
aplasia/hypoplasia affecting the retina Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the retina Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
angioid streaks of the retina Gene Set From HPO Gene-Disease Associations genes associated with the angioid streaks of the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neovascularization of peripheral and posterior retina Gene Set From HPO Gene-Disease Associations genes associated with the neovascularization of peripheral and posterior retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Neural retina-specific leucine zipper protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Neural retina-specific leucine zipper protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
retina microaneurysm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retina microaneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
calcified retina Gene Set From MPO Gene-Phenotype Associations gene mutations causing the calcified retina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent retina Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent retina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased total retina thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased total retina thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retina morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retina outer limiting membrane morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retina outer limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retina coloboma Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retina coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ventral retina size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ventral retina size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retina inner limiting membrane morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retina inner limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal total retina thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retina hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retina hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retina hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[fleck retina, familial benign] Gene Set From OMIM Gene-Disease Associations genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.
gyrate atrophy of choroid and retina with or without ornithinemia Gene Set From OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
doyne honeycomb degeneration of retina Gene Set From OMIM Gene-Disease Associations genes associated with the doyne honeycomb degeneration of retina phenotype from the curated OMIM Gene-Disease Associations dataset.
cavernous malformations of cns and retina Gene Set From OMIM Gene-Disease Associations genes associated with the cavernous malformations of cns and retina phenotype from the curated OMIM Gene-Disease Associations dataset.
retina Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term retina in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
retina Gene Set From ProteomicsDB Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in retina relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.
retina Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retina from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
neural retina Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue neural retina from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
retina Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue retina in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
neural retina Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue neural retina in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
retina Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue retina in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Eye-retina horizontal cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retina horizontal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Atrophic Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophic Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coloboma Of Choroid And Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coloboma Of Choroid And Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coloboma Of The Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coloboma Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Avascular Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Avascular Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cavernous Hemangioma Of Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cavernous Hemangioma Of Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Capillary Hemangioma Of Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Capillary Hemangioma Of Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Traction Detachment Of Retina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Traction Detachment Of Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Retina, Familial Benign Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Retina, Familial Benign in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bone Spicule Pigmentation Of The Retina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bone Spicule Pigmentation Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Yellow/White Lesions Of The Retina Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Yellow/White Lesions Of The Retina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
retina homeostasis Gene Set From GO Biological Process Annotations 2023 genes participating in the retina homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of neural retina development Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of neural retina development biological process from the curated GO Biological Process Annotations 2023 dataset.
embryonic retina morphogenesis in camera-type eye Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset.
retina vasculature development in camera-type eye Gene Set From GO Biological Process Annotations 2023 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset.
CRX-20693478-ADULT-RETINA-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the CRX-20693478-ADULT-RETINA-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
CRX-20693478-RETINA-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the CRX-20693478-RETINA-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
CCND1-20090754-RETINA-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the CCND1-20090754-RETINA-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
abnormal retina neuronal layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina neuronal layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina pigment epithelium morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina pigment epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina photoreceptor layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina photoreceptor layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina pigment epithelium hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina pigment epithelium hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
disorganized retina layers Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized retina layers phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina photoreceptor morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina photoreceptor morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina outer nuclear layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina outer nuclear layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina neovascularization Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina neovascularization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased retina photoreceptor cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased retina photoreceptor cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina vasculature morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina vasculature morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina deposits Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina photoreceptor degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina photoreceptor degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina outer nuclear layer degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina outer nuclear layer degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin retina outer nuclear layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina outer nuclear layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased retina apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retina apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina rod cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina rod cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina outer plexiform layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina outer plexiform layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased total retina thickness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased total retina thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina fold Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina fold phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina outer limiting membrane morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina outer limiting membrane morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina ganglion layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina ganglion layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina detachment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina detachment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina inner nuclear layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner nuclear layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina cone bipolar cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina cone bipolar cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina rod bipolar cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina rod bipolar cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina ganglion cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina ganglion cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased retina cone cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased retina cone cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin retina inner nuclear layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina inner nuclear layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina gliosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina gliosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina inner plexiform layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner plexiform layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina nerve fiber layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina nerve fiber layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina ganglion layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina ganglion layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal induced retina neovascularization Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal induced retina neovascularization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina ganglion cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina ganglion cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina cone cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina cone cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina rod cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina rod cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina spots Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina spots phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin retina inner plexiform layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin retina outer plexiform layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina outer plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina rod cell inner segment morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina rod cell inner segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina rod cell outer segment morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina rod cell outer segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina pigmentation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased retina apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased retina apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
disorganized retina ganglion layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized retina ganglion layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
disorganized retina inner nuclear layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized retina inner nuclear layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
disorganized retina outer nuclear layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized retina outer nuclear layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased total retina thickness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased total retina thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina cone cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina cone cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina cone cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina cone cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina progenitor cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina progenitor cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased retina ganglion cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased retina ganglion cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin retina ganglion layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin retina ganglion layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina pigment epithelium atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina pigment epithelium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to induced retina damage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced retina damage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina cone cell outer segment morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina cone cell outer segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina horizontal cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina horizontal cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina fibrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina bipolar cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina bipolar cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina rod cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina rod cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina horizontal cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina horizontal cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased ventral retina size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ventral retina size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased retina photoreceptor cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retina photoreceptor cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
disorganized retina outer plexiform layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized retina outer plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased retina ganglion cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retina ganglion cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina inner plexiform layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
calcified retina Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified retina phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina melanin granule morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina melanin granule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased retina rod cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased retina rod cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased retina cone cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retina cone cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina ischemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina ischemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina blood vessel morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina blood vessel morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina microaneurysm Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina microaneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal blood-retina barrier function Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood-retina barrier function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina inner limiting membrane morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner limiting membrane morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent retina ganglion cell Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent retina ganglion cell phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thick retina ganglion layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thick retina ganglion layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina cone cell inner segment morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina cone cell inner segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina coloboma Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina coloboma phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thick retina inner plexiform layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thick retina inner plexiform layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina inner nuclear layer thickness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina inner nuclear layer thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal total retina thickness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal total retina thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptilbility to retina ischemic injury Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptilbility to retina ischemic injury phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina outer nuclear layer thickness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina outer nuclear layer thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
serous retina detachment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the serous retina detachment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina ganglion cell dendrite morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina ganglion cell dendrite morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptilbility to retina ischemic injury Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptilbility to retina ischemic injury phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased retina rod cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retina rod cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased retina vascular tortuosity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retina vascular tortuosity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina artery morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina melanocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina melanocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal retina morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal retina outer nuclear layer morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal retina outer nuclear layer morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
decreased total retina thickness Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased total retina thickness phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal retina inner nuclear layer morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal retina inner nuclear layer morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal retina blood vessel morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal retina blood vessel morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal retina vasculature morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal retina vasculature morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
increased total retina thickness Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased total retina thickness phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Neural retina cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Neural retina cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retina cell_Retina_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retina cell_Retina_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retina ganglion cell_Eye_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retina ganglion cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
retina homeostasis Gene Set From GO Biological Process Annotations 2025 genes participating in the retina homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of neural retina development Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of neural retina development biological process from the curated GO Biological Process Annotations 2025 dataset.
embryonic retina morphogenesis in camera-type eye Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset.
retina vasculature development in camera-type eye Gene Set From GO Biological Process Annotations 2025 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset.
Retina lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retina lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial benign fleck retina Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial benign fleck retina in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retina Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retina from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Neural retina Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Neural retina from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Retina Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Retina in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Retina Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Retina in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Neural retina Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Neural retina in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Gyrate atrophy of choroid and retina Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gyrate atrophy of choroid and retina phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Trichomegaly-retina pigmentary degeneration-dwarfism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duchenne muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular dystrophy, vitelliform, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular dystrophy, vitelliform, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asphyxiating thoracic dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fleck corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Occult macular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Occult macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2S Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular corneal dystrophy Type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bietti crystalline corneoretinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bietti crystalline corneoretinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy Type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone dystrophy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thiel-Behnke corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reis-Bucklers' corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy, X-linked 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitelliform dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vitelliform dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy, fuchs endothelial, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal dystrophy Fuchs endothelial 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy Fuchs endothelial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schnyder crystalline corneal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONE DYSTROPHY 5, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONE DYSTROPHY 5, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy type 3A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile neuroaxonal dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular dystrophy, vitelliform, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular dystrophy, vitelliform, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal endothelial dystrophy type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal endothelial dystrophy type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy amelogenesis imperfecta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lattice corneal dystrophy Type III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cone-rod dystrophy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cone-rod dystrophy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Groenouw corneal dystrophy type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Corneal epithelial dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal epithelial dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Stromal Corneal Dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miyoshi Muscular Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, gelatinous drop-like Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral muscular dystrophy 1a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, retinal, 1, North Carolina type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 8 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 7 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 5 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy Avellino type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 6 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 3 from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, atypical vitelliform Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, atypical vitelliform from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, concentric annular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, concentric annular from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 13 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Animal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Endothelial, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset.
Macular Dystrophy, Retinal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.
Lattice corneal dystrophy type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Fuchs' endothelial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 2 from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Bullous Dystrophy, Hereditary Macular Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Reflex Sympathetic Dystrophy from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Crystalline, of Schnyder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Crystalline, of Schnyder from the curated CTD Gene-Disease Associations dataset.
Scleroatonic muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scleroatonic muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone Dystrophy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Fuchs' endothelial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Lisch Epithelial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lisch Epithelial from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, epithelial basement membrane Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, epithelial basement membrane from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy and perceptive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.
MACULAR DYSTROPHY, RETINAL, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bothnia Retinal Dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy, X-Linked, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy, X-Linked, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 3 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Corneal endothelial dystrophy type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal endothelial dystrophy type 2 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 9 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 2 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.
Doyne honeycomb retinal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.
Bietti Crystalline Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bietti Crystalline Dystrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.
OCCULT MACULAR DYSTROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OCCULT MACULAR DYSTROPHY from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset.
Asphyxiating Thoracic Dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Oculopharyngeal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fleck Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fleck from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Merosin-Positive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.
Retinal cone dystrophy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby from the curated CTD Gene-Disease Associations dataset.
Myotonic Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myotonic Dystrophy from the curated CTD Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy, limb-girdle, type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 7 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.
Limb-girdle muscular dystrophy type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Posterior Polymorphous, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 from the curated CTD Gene-Disease Associations dataset.
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitelliform Macular Dystrophy from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Congenital Stromal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
Choroidal dystrophy central areolar Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy, Thiel-Behnke type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 12 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 11 from the curated CTD Gene-Disease Associations dataset.
Cone-Rod Dystrophy 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cone-Rod Dystrophy 10 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY, X-LINKED, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY, X-LINKED, 1 from the curated CTD Gene-Disease Associations dataset.
Newfoundland Rod-Cone Dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Newfoundland Rod-Cone Dystrophy from the curated CTD Gene-Disease Associations dataset.
Groenouw type I corneal dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset.
CONE-ROD DYSTROPHY 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONE-ROD DYSTROPHY 15 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Lattice Type IIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.
Retinal Cone Dystrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 5 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.
Corneal Dystrophy, Fuchs Endothelial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 4 from the curated CTD Gene-Disease Associations dataset.
Corneal dystrophy of Bowman layer, type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset.
Macular dystrophy, corneal type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Lmna-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.
Fuchs Endothelial Dystrophy Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease oculopharyngeal muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease facioscapulohumeral muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cone-rod dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
asphyxiating thoracic dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
vitelliform macular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial central choroid dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial central choroid dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lattice corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
oculopharyngeal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oculopharyngeal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitelliform macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitelliform macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal granular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal granular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
facioscapulohumeral muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease facioscapulohumeral muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary retinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease limb-girdle muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reflex sympathetic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reflex sympathetic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ullrich congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ullrich congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vulvar dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
occult macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease occult macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fuchs' endothelial dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fuchs' endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
becker muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease becker muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cone-rod dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cone-rod dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
macular corneal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
emery-dreifuss muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease emery-dreifuss muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
asphyxiating thoracic dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease asphyxiating thoracic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bietti crystalline corneoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bietti crystalline corneoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neuroaxonal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuroaxonal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fundus dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fundus dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fukuyama congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fukuyama congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitreoretinal dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitreoretinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
duchenne muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease duchenne muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular dystrophy-dystroglycanopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular dystrophy-dystroglycanopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myotonic dystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cone dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cone dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
granular corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease granular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fuchs endothelial dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fuchs endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gelatinous droplike corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gelatinous droplike corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic dystrophy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular corneal dystrophy. Gene Set From GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
corneal dystrophies, hereditary; hereditary corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mental retardation; muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, oculopharyngeal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, oculopharyngeal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinitis pigmentosa; macular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease retinitis pigmentosa; macular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrioventricular block; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrioventricular block; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease ullrich congenital muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome disorders; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome disorders; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fuchs' endothelial dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fuchs' endothelial dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lattice corneal dystrophy type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone-rod dystrophy; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease cone-rod dystrophy; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibromyalgia; myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease fibromyalgia; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recessive cone-rod dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease recessive cone-rod dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene Set From GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotonic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular corneal dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophy, duchenne Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystrophy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dystrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Fuchs's corneal dystrophy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
corneal dystrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease corneal dystrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
nail dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nail dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polymorphous posterior corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the polymorphous posterior corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lattice corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the lattice corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb-girdle muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the cone-rod dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macroreticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macroreticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
granular corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the granular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
map-dot-fingerprint corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the map-dot-fingerprint corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
speckled corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the speckled corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
crystalline corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the crystalline corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the choroidal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
marginal corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the marginal corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nodular corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nodular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive congenital retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive congenital retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
juvenile epithelial corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the juvenile epithelial corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the macular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mosaic corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the mosaic corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the punctate corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reticular retinal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the reticular retinal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital muscular dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the congenital muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corneal dystrophy Gene Set From HPO Gene-Disease Associations genes associated with the corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex Sympathetic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Emery-Dreifuss Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Vitelliform Macular Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Vitelliform Macular Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Facioscapulohumeral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Facioscapulohumeral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myotonic Dystrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myotonic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Dystrophy, Duchenne Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Dystrophy, Duchenne phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myotonic dystrophy protein kinase, coiled coil Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Myotonic dystrophy protein kinase, coiled coil protein domain from the InterPro Predicted Protein Domain Annotations dataset.
nail dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nail dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axonal dystrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
corneal dystrophy, schnyder type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset.
fascioscapulohumeral muscular dystrophy 2, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
newfoundland rod-cone dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the newfoundland rod-cone dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
bothnia retinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, megaconial type Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.
t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, congenital alopecia, and nail dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
occult macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset severe Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract with late-onset corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2c Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, congenital stromal Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, congenital stromal phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lattice type iiia Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy, x-linked, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, gelatinous drop-like Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, gelatinous drop-like phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod retinal dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, retinal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 6, 60177 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 6, 60177 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, fuchs endothelial, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to itga7 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy, limb-girdle, type 2r Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
toenail dystrophy, isolated Gene Set From OMIM Gene-Disease Associations genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, rigid spine, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, epithelial basement membrane Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, epithelial basement membrane phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, merosin-positive Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2q Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2s Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2d Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2g Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2l Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 2j Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.
hypotrichosis, congenital, with juvenile macular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the hypotrichosis, congenital, with juvenile macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
ullrich congenital muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy and perceptive deafness Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy and perceptive deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, north carolina type Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, north carolina type phenotype from the curated OMIM Gene-Disease Associations dataset.
tibial muscular dystrophy, tardive Gene Set From OMIM Gene-Disease Associations genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinol dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the retinol dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1h Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 1, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
oculopharyngeal muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, reis-bucklers type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
miyoshi muscular dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the miyoshi muscular dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, patterned, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, patterned, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 4 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3 Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, thiel-behnke type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, thiel-behnke type phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy with central cone involvement Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy, progressive x-linked, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
choriodal dystrophy, central areolar 2 Gene Set From OMIM Gene-Disease Associations genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonic dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myotonic dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myotonic dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myotonic dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, endothelial, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
cone-rod dystrophy 20 Gene Set From OMIM Gene-Disease Associations genes associated with the cone-rod dystrophy 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
duchenne muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile neuroaxonal dystrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 3, ar Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal endothelial dystrophy 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
limb-girdle muscular dystrophy, type 1g Gene Set From OMIM Gene-Disease Associations genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.
sorsby fundus dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the sorsby fundus dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with rimmed vacuoles Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
bietti crystalline corneoretinal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 6, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy with epidermolysis bullosa simplex Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lattice type i Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type i phenotype from the curated OMIM Gene-Disease Associations dataset.
vitelliform macular dystrophy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the vitelliform macular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 1, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
becker muscular dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, posterior polymorphous 2 Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, groenouw type i Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
meesmann corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal fleck dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the corneal fleck dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
macular corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1e Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1f Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1a Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, limb-girdle, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
?cone-rod dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
emery-dreifuss muscular dystrophy 7, ad Gene Set From OMIM Gene-Disease Associations genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital merosin-deficient Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal cone dystrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal cone dystrophy 3b Gene Set From OMIM Gene-Disease Associations genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, avellino type Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset.
corneal dystrophy, lisch epithelial Gene Set From OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lisch epithelial phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular dystrophy, vitelliform, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular dystrophy, vitelliform, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
Emery-Dreifuss muscular dystrophy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
myotonic dystrophy type1 Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease myotonic dystrophy type1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Bietti Crystalline Corneoretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bietti Crystalline Corneoretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
North Carolina Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease North Carolina Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myotonic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotonic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fleck Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fleck Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obsolete Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obsolete Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Avellino Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Avellino Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophy, Granular Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophy, Granular in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Or Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Or Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiel-Behnke Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiel-Behnke Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eichsfeld Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eichsfeld Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fuchs Endothelial Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fuchs Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lattice Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lattice Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miyoshi Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne And Becker Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne And Becker Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Walker-Warburg Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Walker-Warburg Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fukuyama Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fukuyama Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Cervical Sympathetic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Cervical Sympathetic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Schnyder Crystalline Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Schnyder Crystalline Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymorphous Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Best Vitelliform Macular Dystrophy, Multifocal (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Best Vitelliform Macular Dystrophy, Multifocal (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile-Onset Vitelliform Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile-Onset Vitelliform Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ullrich Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ullrich Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myotonic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myotonic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reflex Sympathetic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reflex Sympathetic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Doyne Honeycomb Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doyne Honeycomb Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Limb Girdle Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Limb Girdle Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy, Tardive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy, Tardive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenintal Hereditary Endothelial Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenintal Hereditary Endothelial Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jeune Thoracic Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jeune Thoracic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mosaic Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mosaic Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Corneal Dystrophy Type Ii (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy Type Ii (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Recurrent Erosion Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Recurrent Erosion Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hereditary Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hereditary Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Toenail Dystrophy, Isolated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toenail Dystrophy, Isolated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Concentric Annular Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Concentric Annular Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Butterfly-Shaped Pigmentary Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Butterfly-Shaped Pigmentary Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patterned Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patterned Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Marginal Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Marginal Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duchenne Muscular Dystrophy, Mental Retardation, And Absence Of Erg B-Wave in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intermediate Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intermediate Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe [Duchenne] Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe [Duchenne] Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facioscapulohumeral Muscular Dystrophy 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facioscapulohumeral Muscular Dystrophy 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cone Dystrophy With Supernormal Rod Response Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cone Dystrophy With Supernormal Rod Response in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Occult Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Occult Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmentary Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmentary Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emery-Dreifuss Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emery-Dreifuss Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Granular Dystrophy, Corneal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Granular Dystrophy, Corneal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreoretinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreoretinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ocular Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ocular Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Choroidal Dystrophy, Central Areolar 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Choroidal Dystrophy, Central Areolar 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Sclerosing Bone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Sclerosing Bone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tibial Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tibial Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1A in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Infantile Neuroaxonal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Infantile Neuroaxonal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Speckled Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Speckled Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Dystrophy, Spinocerebellar Ataxia, And Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pre-Descemet'S Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pre-Descemet'S Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bull'S Eye Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bull'S Eye Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Dystrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Dystrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bothnia Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bothnia Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Newfoundland Rod-Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Newfoundland Rod-Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Biallelic Rpe65 Mutation Associated Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Biallelic Rpe65 Mutation Associated Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gelatinous Droplike Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gelatinous Droplike Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epithelial Basement Membrane Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Basement Membrane Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Groenouw Corneal Dystrophy Type I (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Groenouw Corneal Dystrophy Type I (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Punctate Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Punctate Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reis-Bucklers' Corneal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reis-Bucklers' Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Salzmann Nodular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Salzmann Nodular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophy Of Vulva Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophy Of Vulva in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nodular Corneal Dystrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nodular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nail dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nail dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purkinje cell axonal dystrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Purkinje cell axonal dystrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Affected pathways in Duchenne muscular dystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Affected pathways in Duchenne muscular dystrophy pathway from the WikiPathways Pathways 2024 dataset.
Muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
limb-girdle muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Emery-Dreifuss muscular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Emery-Dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
cone-rod dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease cone-rod dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Gelatinous drop-like corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gelatinous drop-like corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
epithelial-stromal TGFBI dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease epithelial-stromal TGFBI dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Epithelial and subepithelial dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Epithelial and subepithelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Lattice corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lattice corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Granular corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Granular corneal dystrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital merosin-deficient muscular dystrophy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital merosin-deficient muscular dystrophy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Meesmann corneal dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Meesmann corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Asphyxiating thoracic dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Vitelliform macular dystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Vitelliform macular dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Harmonizome 3.0

EEGV1 Gene

MDRV Gene

MCDR3 Gene

MCDR1 Gene

MCDR4 Gene

CYMD Gene

LGMD1H Gene

LGMD1G Gene

FECD7 Gene

FECD5 Gene

FECD3 Gene

FECD2 Gene

MDC1B Gene

VMD1 Gene

CDB2 Gene

CACD Gene

COD2 Gene

FSHMD1A Gene

FSHMD1B Gene

CORD8 Gene

CORD1 Gene

CORD4 Gene

CACD3 Gene

LECD Gene

MDBS2 Gene

RCD1 Gene

CORD17 Gene

ATD Gene

MDCMP Gene

XECD Gene

CHED1 Gene

Pattern Dystrophy Of The Retina Gene Set

abnormal retina blood vessel pattern Gene Set

Multifocal Pattern Dystrophy Of Retinal Pigment Epithelium Simulating Fundus Flavimaculatus Gene Set

Multifocal pattern dystrophy simulating fundus flavimaculatus Gene Set

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

male-pattern baldness Gene Set

male pattern baldness Gene Set

polycystic ovaries and premature male pattern baldness Gene Set

pattern Gene Set

embryonic heart tube anterior/posterior pattern specification Gene Set

proximal/distal pattern formation involved in nephron development Gene Set

regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

anterior compartment pattern formation Gene Set

cytoplasmic pattern recognition receptor signaling pathway in response to virus Gene Set

pattern specification involved in kidney development Gene Set

proximal/distal pattern formation involved in metanephric nephron development Gene Set

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

anterior/posterior pattern specification involved in kidney development Gene Set

negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

lung pattern specification process Gene Set

neural plate pattern specification Gene Set

cell fate commitment involved in pattern specification Gene Set

anterior/posterior pattern specification Gene Set

compartment pattern specification Gene Set

cell fate specification involved in pattern specification Gene Set

pattern recognition receptor signaling pathway Gene Set

embryonic pattern specification Gene Set

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

pattern specification involved in metanephros development Gene Set

forebrain dorsal/ventral pattern formation Gene Set

radial pattern formation Gene Set

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

dorsal/ventral pattern formation Gene Set

pattern specification involved in mesonephros development Gene Set

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

left/right pattern formation Gene Set

cytoplasmic pattern recognition receptor signaling pathway Gene Set

cell surface pattern recognition receptor signaling pathway Gene Set

pattern specification process Gene Set

anterior/posterior pattern specification involved in ureteric bud development Gene Set

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

forebrain anterior/posterior pattern specification Gene Set

embryonic heart tube left/right pattern formation Gene Set

pattern specification involved in pronephros development Gene Set

proximal/distal pattern formation Gene Set

cell fate determination involved in pattern specification Gene Set

signaling pattern recognition receptor activity Gene Set