| Name |
|---|
AAA1 Geneaortic aneurysm, familial abdominal 1 |
AAA2 GeneAortic aneurysm, familial abdominal 2 |
AAA4 GeneAortic aneurysm, familial abdominal, 4 |
AAT2 GeneAortic aneurysm, familial thoracic 2 |
AAT1 GeneAortic aneurysm, familial thoracic 1 |
PTLAH Genepatella aplasia-hypoplasia |
AMMECR1 GeneAlport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010] |
AMMEC GeneAlport syndrome, mental retardation, midface hypoplasia, and elliptocytosis |
FHASD GeneFoveal hypoplasia and anterior segment dysgenesis |
CHMRQ GeneCerebellar hypoplasia, mental retardation, and quadrupedal locomotion |
IHG1 Geneiris hypoplasia with glaucoma 1 |
MCOPCT1 Genecataract, congenital, with microphthalmia |
CFTDX GeneMyopathy, congenital, with fiber-type disproportion, X-linked |
NPHS1 Genenephrosis 1, congenital, Finnish type (nephrin) This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009] |
CTRCT37 GeneCataract, congenital cerulean type, 5 |
CTRCT34 GeneCataract, autosomal recessive congenital 3 |
CTRCT35 Genecataract, congenital nuclear, autosomal recessive |
BSCL2 GeneBerardinelli-Seip congenital lipodystrophy 2 (seipin) This gene encodes the multi-pass transmembrane protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2).[provided by RefSeq, Jul 2024] |
HTC1 Genehypertrichosis 1 (universalis, congenital) |
HTC2 Genehypertrichosis 2 (generalized, congenital) |
RNANC GeneRetinal nonattachment, nonsyndromic congenital |
NHS GeneNance-Horan syndrome (congenital cataracts and dental anomalies) This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2014] |
MDC1B GeneMuscular dystrophy, congenital, 1B |
CDAN3 Genecongenital dyserythropoietic anemia, type III |
LCA5L GeneLeber congenital amaurosis 5-like Predicted to be involved in intraciliary transport. Predicted to be active in axoneme. [provided by Alliance of Genome Resources, Mar 2025] |
NDNC9 GeneNail disorder, nonsyndromic congenital, 9 |
NYS2 Genenystagmus 2, congenital autosomal dominant |
NYS3 Genenystagmus 3, congenital autosomal dominant |
NYS7 GeneNystagmus 7, congenital |
NYS4 Genenystagmus 4, congenital autosomal dominant |
NDIC GeneNail dysplasia, isolated congenital |
CTRCT27 GeneCataract, congenital, nuclear progressive |
PTOS2 GenePtosis, hereditary congenital 2 |
PTOS1 Geneptosis, congenital 1 (autosomal dominant) |
GLC3C Geneglaucoma 3, primary congenital, C |
SMAL Genespinal muscular atrophy, congenital nonprogressive, of lower limbs |
ANIC GeneAnosmia, isolated congenital |
CHDT3 GeneCongenital heart defects, multiple types, 3 |
MDCMP Genemuscular dystrophy, congenital, merosin-positive |
CHNG3 GeneHypothyroidism, congenital, nongoitrous, 3 |
LCA5 GeneLeber congenital amaurosis 5 This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009] |
CCA1 Genecataract, congenital, cerulean type, 1 |
CCT Genecataract, congenital, total |
CCV Genecataract, congenital, Volkmann type |
MCOR Genemicrocoria, congenital |
DIH2 GeneHernia, congenital diaphragmatic 2 |
ARCI9 GeneIchthyosis, congenital, autosomal recessive 9 |
ARCI7 GeneIchthyosis, congenital, autosomal recessive 7 |
PAFC GenePreauricular fistulae, congenital |
Congenital Hypoplasia Of Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic arch hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Congenital Anomaly Of Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomaly Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations 2015 dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom 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. |
right aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the right aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
coarctation of the descending aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the coarctation of the descending aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interrupted aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the interrupted aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
right aortic arch with mirror image branching Gene SetFrom HPO Gene-Disease Associations genes associated with the right aortic arch with mirror image branching phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
right aortic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the right aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
double aortic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the double aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
calcified aortic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the calcified aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
interrupted aortic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the interrupted aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cervical aortic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cervical aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
interrupted aortic arch, type b Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the interrupted aortic arch, type b phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic arch coarctation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic arch coarctation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Right Aortic Arch (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Right Aortic Arch (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Interrupted Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Interrupted Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Right Aortic Arch With Mirror Image Branching Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Right Aortic Arch With Mirror Image Branching in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Arch Calcification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Arch Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Left Aortic Arch With Retroesophageal Right Subclavian Artery Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Aortic Arch With Retroesophageal Right Subclavian Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal aortic arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
interrupted aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the interrupted aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic arch coarctation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch coarctation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
right aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the right aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cervical aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cervical aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
interrupted aortic arch, type b Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the interrupted aortic arch, type b phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic arch development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
calcified aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double lumen aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double lumen aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic arch dilation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch dilation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Aortic arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
pharyngeal arch artery hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pharyngeal arch artery hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
first pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the first pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
zygomatic arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the zygomatic arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fourth pharyngeal arch artery hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fourth pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fourth pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fourth pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
third pharyngeal arch artery hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the third pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
second pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the second pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipids; left ventricular mass; aortic gradient; aortic valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipids; left ventricular mass; aortic gradient; aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, thoracic; aortic rupture Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, thoracic; aortic rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; aortic rupture Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial thoracic aortic aneurysm and aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial thoracic aortic aneurysm and aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bicuspid aortic valve without aortic dilation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve without aortic dilation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Congenital Stenosis Of Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Stenosis Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Supravalvular Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Supravalvular Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Atresia Of Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital adrenal hypoplasia, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ADRENAL HYPOPLASIA, CONGENITAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset. |
isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism Gene SetFrom OMIM Gene-Disease Associations genes associated with the adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Lung Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Penis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Penis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Adrenal Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Femur Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Thymus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Thymus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Radius Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Radius in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Tricuspid Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Tricuspid Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Clavicle Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Clavicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Thyroid Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Thyroid Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Pulmonary Artery Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Pulmonary Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Erythroid Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Erythroid Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Renal Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Renal Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Part Of Brain Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Part Of Brain in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pancreatic hypoplasia-diabetes-congenital heart disease syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital pontocerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital pontocerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital adrenal hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital adrenal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancreatic hypoplasia-diabetes-congenital heart disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
congenital heart defects; heart defects, congenital; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; folic acid deficiency; heart defects, congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; heart defects, congenital; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; heart defects, congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; heart defects, congenital; nervous system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Heart Defects, Congenital, And Other Congenital Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
arch Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term arch in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
pharyngeal arch artery morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pharyngeal arch artery morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
butterfly vertebral arch Gene SetFrom HPO Gene-Disease Associations genes associated with the butterfly vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vertebral arch anomaly Gene SetFrom HPO Gene-Disease Associations genes associated with the vertebral arch anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cleft vertebral arch Gene SetFrom HPO Gene-Disease Associations genes associated with the cleft vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the zygomatic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the zygomatic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
rRNA-processing arch domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the rRNA-processing arch domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fused first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the fused first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pharyngeal arch arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pharyngeal arch arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertebral arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent fourth pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent fourth pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zygomatic arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zygomatic arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent vertebral arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent zygomatic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent zygomatic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fourth pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fourth pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small second pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small second pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pharyngeal arch arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pharyngeal arch arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fourth pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fourth pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal third pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal third pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ectopic pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ectopic pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal second pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal second pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal second pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal second pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent third pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent third pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sixth pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sixth pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal third pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal third pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertebral arch development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent sixth pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent sixth pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch artery stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal first pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent second pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent second pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sixth pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sixth pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
neural arch Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue neural arch from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
branchial arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue branchial arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
neural arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue neural arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
gill arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue gill arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Byzanthine Arch Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Byzanthine Arch Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vertebral Arch Anomaly Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vertebral Arch Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Butterfly Vertebral Arch Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Butterfly Vertebral Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
pharyngeal arch artery morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the pharyngeal arch artery morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small second pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small second pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vertebral arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fourth pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fourth pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal third pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal third pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vertebral arch development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal zygomatic arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zygomatic arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal first pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal first pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent second pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent second pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent pharyngeal arch arteries Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent pharyngeal arch arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent second pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent second pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent third pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent third pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mandibular dental arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mandibular dental arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent vertebral arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pharyngeal arch artery stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fourth pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fourth pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sixth pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sixth pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
persistent right 6th pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the persistent right 6th pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal second pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal second pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal second pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal second pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal third pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal third pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch mesenchyme morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch mesenchyme morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sixth pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sixth pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent third pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent third pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent fourth pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent fourth pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sixth pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sixth pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal maxillary dental arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary dental arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent fourth pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent fourth pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ectopic pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sixth pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sixth pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated third pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated third pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vertebral arch morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal vertebral arch morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal pharyngeal arch morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal pharyngeal arch morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Pharyngeal arch mesenchyme cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pharyngeal arch mesenchyme cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pharyngeal arch cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pharyngeal arch cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pharyngeal arch 1 mesenchyme cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pharyngeal arch 1 mesenchyme cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
pharyngeal arch artery morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the pharyngeal arch artery morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
Neural arch Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Neural arch from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Branchial arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Branchial arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Neural arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Neural arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Gill arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Gill arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Pharyngeal arch cartilage Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Pharyngeal arch cartilage in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
sporadic abdominal aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the sporadic abdominal aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Supravalvar aortic stenosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Supravalvar aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic valve disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic valve disorder Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic Aneurysm, Familial Abdominal 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset. |
Aortic Valve, Calcification of Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Valve, Calcification of from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Abdominal 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset. |
Aortic Stenosis, Subvalvular Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Stenosis, Subvalvular from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Thoracic from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Abdominal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Abdominal from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm from the curated CTD Gene-Disease Associations dataset. |
Aortic Valve Insufficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Valve Insufficiency from the curated CTD Gene-Disease Associations dataset. |
Aortic Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Diseases from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset. |
Aortic Rupture Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Rupture from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset. |
Aortic aneurysm, familial thoracic 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset. |
AORTIC VALVE DISEASE 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AORTIC VALVE DISEASE 1 from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Abdominal 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset. |
Aortic Stenosis, Supravalvular Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Stenosis, Supravalvular from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Abdominal Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Aortic Aneurysm, Abdominal in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Aortic Aneurysm, Thoracic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
supravalvular aortic stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic valve stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic valve stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic aneurysm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic valve disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic valve disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
aortic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic atherosclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve prolapse Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve prolapse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thoracic aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
supravalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease supravalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abdominal aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abdominal aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
subvalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subvalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
H3K4me3_fibroblast of the aortic adventitia_hg19_2 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of the aortic adventitia_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
H3K4me3_fibroblast of the aortic adventitia_hg19_1 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of the aortic adventitia_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
CTCF_fibroblast of the aortic adventitia_hg19_1 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of the aortic adventitia_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
CTCF_fibroblast of the aortic adventitia_hg19_2 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of the aortic adventitia_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
coronary artery disease; aortic stiffness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; aortic stiffness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
calcific aortic valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcific aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, thoracic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, thoracic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic diseases; calcinosis; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic diseases; calcinosis; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; inflammation; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; inflammation; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve insufficiency; rheumatic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve insufficiency; rheumatic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, ruptured; aortic aneurysm, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal aortic aneurysm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal aortic aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; calcinosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; lung cancer; abdominal aortic aneurysm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; lung cancer; abdominal aortic aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic stiffness and disease severity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic stiffness and disease severity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, ruptured; aortic aneurysm, abdominal; arterial occlusive diseases; carotid artery stenosis; carotid stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal; arterial occlusive diseases; carotid artery stenosis; carotid stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic atherosclerosis in diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic atherosclerosis in diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, abdominal aortic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, abdominal aortic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
supravalvular aortic stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease supravalvular aortic stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic diseases; calcinosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic diseases; calcinosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; calcinosis; diabetes mellitus; hyperlipidemias; hypertension; mitral valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis; diabetes mellitus; hyperlipidemias; hypertension; mitral valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic diseases; calcinosis; hyperlipoproteinemia type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic diseases; calcinosis; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic stiffness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic stiffness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; arterial occlusive diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; arterial occlusive diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic root size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic root size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve insufficiency; calcinosis; mitral valve insufficiency; rheumatic heart disease; tricuspid valve insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve insufficiency; calcinosis; mitral valve insufficiency; rheumatic heart disease; tricuspid valve insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
differential expansion rates of small abdominal aortic aneurysms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease differential expansion rates of small abdominal aortic aneurysms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term aortic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
LOX-1_OE_GDS4262_433_human_HAECT - aortic endothelial cell line - 6 Hours Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_433_human_HAECT - aortic endothelial cell line - 6 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
LOX-1_OE_GDS4262_434_human_HAECT - aortic endothelial cell line - 12 Hours Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_434_human_HAECT - aortic endothelial cell line - 12 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
LOX-1_OE_GDS4262_435_human_HAECT - aortic endothelial cell line - 24 Hours Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_435_human_HAECT - aortic endothelial cell line - 24 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
LOX-1_OE_GDS4262_432_human_HAECT - aortic endothelial cell line - 2 Hours Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_432_human_HAECT - aortic endothelial cell line - 2 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
aortic valve morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Abdominal aortic aneurysm Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Abdominal aortic aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Thoracic aortic aneurysms and dissections Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Aortic-valve calcification Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Aortic-valve calcification phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Aortic root size Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abdominal aortic aneurysm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease abdominal aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
aortic disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease aortic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
thoracic aortic aneurysm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease thoracic aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
aortic valve disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease aortic valve disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
aortic aneurysm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abdominal aortic aneurysm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abdominal aortic aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aortic valve calcification Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aortic valve calcification phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
bicuspid aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the bicuspid aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aortic aneurysm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aortic aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aortic dilatation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aortic dilatation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aortic regurgitation Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic regurgitation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic tortuosity Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic root dilatation Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic root dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic valve stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic valve stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
calcific aortic valve stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the calcific aortic valve stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic valve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
descending aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the descending aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic dissection Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic dissection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ascending aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the ascending aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic valve atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic valve atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ascending aortic dissection Gene SetFrom HPO Gene-Disease Associations genes associated with the ascending aortic dissection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bicuspid aortic valve Gene SetFrom HPO Gene-Disease Associations genes associated with the bicuspid aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
supravalvular aortic stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the supravalvular aortic stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic valve calcification Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic valve calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aortic dilatation Gene SetFrom HPO Gene-Disease Associations genes associated with the aortic dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dissecting aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the dissecting aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm, Thoracic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Aneurysm, Abdominal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm, Abdominal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Valve Insufficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Valve Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Aneurysm Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Rupture Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Rupture phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Stenosis, Supravalvular Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Stenosis, Supravalvular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Valve Stenosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Valve Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Coarctation Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Coarctation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
aortic valve atresia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic valve anulus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic valve anulus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic valve stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
calcified aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the calcified aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic dissection Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic dissection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic sinus aneurysm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic sinus aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic valve cusp morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic valve cusp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic hypertrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick aortic valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic sac morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic sac morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic aneurysm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
bicuspid aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the bicuspid aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent aortic valve cusps Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent aortic valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic valve regurgitation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic valve regurgitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
supravalvar aortic stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the supravalvar aortic stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
patent aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the patent aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated aortic sac Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated aortic sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
overriding aortic valve Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the overriding aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic elastic tissue lesions Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic valve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic valve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic aneurysm, familial thoracic 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 9 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial abdominal 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial abdominal 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, ascending, and dissection Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, ascending, and dissection phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic valve disease 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic valve disease 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic valve disease 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic valve disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
supravalvar aortic stenosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the supravalvar aortic stenosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial abdominal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term aortic in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
aortic smooth muscle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue aortic smooth muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
aortic smooth muscle cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic smooth muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
aortic valve Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic valve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
aortic smooth muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic smooth muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
aortic endothelial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic endothelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
porcine aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue porcine aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
human aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue human aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
aortic root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Aortic Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Supravalvular Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Supravalvular Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Dissection Rupture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Dissection Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Insufficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Coarctation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Coarctation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Calcification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Descending Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Descending Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dissecting Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Rupture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Senile Sclerosis Of Aortic Cusp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Senile Sclerosis Of Aortic Cusp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Root Dilation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Root Dilation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Wall Hypertrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Wall Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dissecting Abdominal Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Root Dilatation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Root Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Angiosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ruptured Abdominal Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ruptured Thoracic Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Thoracic Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracoabdominal Aortic Aneurysm, Ruptured Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracoabdominal Aortic Aneurysm, Ruptured in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paravalvular Aortic Regurgitation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paravalvular Aortic Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Aortic Valve Physiology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Degenerative Aortic Valve Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Degenerative Aortic Valve Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Aortic Ectasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Aortic Ectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitral And Aortic Incompetence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitral And Aortic Incompetence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Stenosis Symptomatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Stenosis Symptomatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rheumatic Aortic Regurgitation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Aortic Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inflammatory Abdominal Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rheumatic Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Disease 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disease 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Descending Thoracic Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Descending Thoracic Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Two-Raphe Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Two-Raphe Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ascending Aortic Rupture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ascending Aortic Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonrheumatic Aortic (Valve) Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonrheumatic Aortic (Valve) Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Aortic Atherosclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Aortic Atherosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mid Aortic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mid Aortic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Isolated Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Isolated Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Tortuosity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loeys-Dietz Aortic Aneurysm Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loeys-Dietz Aortic Aneurysm Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Disease 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disease 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Intramural Haematoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Intramural Haematoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Quadricuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Quadricuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Unicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Unicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Stiffness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ascending Aortic Dissection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ascending Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ascending Aortic Dilatation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ascending Aortic Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dysplastic Aortic Valve Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysplastic Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aortic Aneurysm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dilated Aortic Root Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilated Aortic Root in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
aortic valve morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
aortic valve development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the aortic valve development biological process from the curated GO Biological Process Annotations 2023 dataset. |
aortic valve formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the aortic valve formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
overriding aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the overriding aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick aortic valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated aortic sac Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated aortic sac phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve regurgitation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve regurgitation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve cusp morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve cusp morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
calcified aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic hypertrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic hypertrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
patent aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the patent aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic dissection Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic dissection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bicuspid aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bicuspid aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve commissure morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve commissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic sinus aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic sinus aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic elastic tissue lesions Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve flow Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve flow phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic sac morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic sac morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased aortic weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased aortic weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent aortic valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve atresia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
supravalvar aortic stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the supravalvar aortic stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve anulus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve anulus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Intra-aortic hematopoietic cell_Embryo_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Intra-aortic hematopoietic cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
aortic valve morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
aortic valve development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the aortic valve development biological process from the curated GO Biological Process Annotations 2025 dataset. |
aortic valve formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the aortic valve formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Aortic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thoracic aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic valve disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Supravalvular aortic stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic valve stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic valve stenosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Abdominal aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve stenosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic valve stenosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic valve disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Thoracic aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic dissection Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic dissection in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic atherosclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Supravalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Supravalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bicuspid aortic valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bicuspid aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic malignant tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic malignant tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve disease 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve disease 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Subvalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subvalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve prolapse Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve prolapse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic smooth muscle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Aortic smooth muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic valve Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic valve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic smooth muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic smooth muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic endothelial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic endothelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic smooth muscle cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic smooth muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Human aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Human aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic body Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic intima Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic intima in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Porcine aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Porcine aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic adventitial fibroblast Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic adventitial fibroblast in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm or dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm or dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic valve disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic valve disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Isolated thoracic aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Supravalvar aortic stenosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Supravalvar aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal aortic valve morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal aortic valve morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic valve atresia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic valve atresia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sporadic abdominal aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sporadic abdominal aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Subvalvular aortic stenosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Subvalvular aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic dilatation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic dilatation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bicuspid aortic valve Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heritable Thoracic Aortic disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Heritable Thoracic Aortic disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early age onset of sporadic thoracic aortic dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early age onset of sporadic thoracic aortic dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ascending aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ascending aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic valve stenosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic valve stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Calcific aortic valve stenosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Calcific aortic valve stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Abdominal aortic aneurysm Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal aortic aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic root size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic valve area Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic valve area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thoracic aortic calcification levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Abdominal aortic calcification levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severe aortic features in Marfan syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe aortic features in Marfan syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic vascular smooth muscle cell proliferation in response to IL-1 beta Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic vascular smooth muscle cell proliferation in response to IL-1 beta phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysms and dissections Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic stiffness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic stiffness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic-valve calcification Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic-valve calcification phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic coarctation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic coarctation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bicuspid aortic valve Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Focal dermal hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Focal dermal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tibia, hypoplasia of, with polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tibia, hypoplasia of, with polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic nerve hypoplasia, bilateral Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Splenic hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Splenic hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Olivopontocerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Olivopontocerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 1b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 2e Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 2e phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Focal Dermal Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Focal Dermal Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset. |
Cartilage-hair hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Leydig Cell Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leydig Cell Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Optic Nerve Hypoplasia, Bilateral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset. |
Polymicrogyria With Optic Nerve Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 2C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2C from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2B from the curated CTD Gene-Disease Associations dataset. |
Anophthalmia with pulmonary hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anophthalmia with pulmonary hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 6 from the curated CTD Gene-Disease Associations dataset. |
PONTOCEREBELLAR HYPOPLASIA, TYPE 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PONTOCEREBELLAR HYPOPLASIA, TYPE 4 from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 1 from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 3 from the curated CTD Gene-Disease Associations dataset. |
Iris hypoplasia and glaucoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset. |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 2A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2A from the curated CTD Gene-Disease Associations dataset. |
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset. |
Foveal Hypoplasia and Anterior Segment Dysgenesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset. |
focal dermal hypoplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease focal dermal hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
dental enamel hypoplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dental enamel hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
focal dermal hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cartilage-hair hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cartilage-hair hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pituitary hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pituitary hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dental enamel hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dental enamel hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypoplasia Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hypoplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aplasia/hypoplasia of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
retinal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of choroid Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the uvula Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tragus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the nose Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
parathyroid hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the parathyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the lungs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lungs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pancreatic hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pancreatic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the quadriceps Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the quadriceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the scapulae Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ventral pons Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ventral pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
glenoid fossa hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the glenoid fossa hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lymph node hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lymph node hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the iris Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior vertebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the lacrimal puncta Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the lacrimal puncta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving forearm bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the nasal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the sternum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the optic nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the corticospinal tracts Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of penis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of penis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic disc hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the optic disc hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thyroid hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the thyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the feet Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the biceps Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the biceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the fundus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the fundus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the retina Gene SetFrom 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. |
aplasia/hypoplasia of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
calf muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the calf muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the gallbladder Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the pelvis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the mandible Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the epiglottis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of metatarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the uterus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
erythroid hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the erythroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pons Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the spleen Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
breast hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the choroid Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ciliary body Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the triceps Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the triceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pharynx Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pharynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
macular hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the macular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pectoralis hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoralis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midclavicular hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the midclavicular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal hypoplasia/aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mandibular condyle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the mandibular condyle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting bones of the axial skeleton Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting bones of the axial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corticospinal tract hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the corticospinal tract hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
carpal bone hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the carpal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal ulnar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the earlobes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the calcaneus Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the calcaneus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 4th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cerebellar vermis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of proximal fibula Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of proximal fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of deltoid muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of deltoid muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 2nd metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the skeleton Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the renal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the uterus Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the humerus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the maxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ribs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 1st metatarsal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the vertebral column Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
laryngeal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the laryngeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal gland hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontal bone hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the frontal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the metacarpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nipples Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 5th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the proximal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the proximal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the premaxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cerebrum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the uvea Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the sweat glands Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
unilateral breast hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the unilateral breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the femur Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pectoralis major hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoralis major hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenal medullary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenal medullary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nasal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the testes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
labial hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the labial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the maxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the optic tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nails Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inferior vermis hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the inferior vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the fovea Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the semicircular canal Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ear cartilage Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ear cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
external genital hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the external genital hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the vagina Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of first ribs Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of first ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar hemisphere hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gonadal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the gonadal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the iris Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
2nd-5th toe middle phalangeal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the 2nd-5th toe middle phalangeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the clavicles Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar vermis hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the sacrum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenocortical hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenocortical hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the skull Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the musculature of the pelvis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized cerebral atrophy/hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tibia Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the prostate Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the prostate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of proximal radius Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of proximal radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the patella Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the lesser trochanter Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the lesser trochanter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the skeletal musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the eyelid Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the vagina Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
unilateral chest hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the unilateral chest hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the breasts Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vertebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the fovea Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic nerve hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the optic nerve hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cervical spine Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cerebellum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hemifacial hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the hemifacial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of dental enamel Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of dental enamel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the lens Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior pituitary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior pituitary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the external ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the shoulder musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the frontal lobes Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the frontal lobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scrotal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the scrotal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intestinal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the intestinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tongue Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
patellar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the patellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the epiglottis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the colon Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fibular hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the fibular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pectoral muscle hypoplasia/aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the macula Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
paranasal sinus hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the paranasal sinus hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
clitoral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the clitoral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the musculature of the thigh Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the fibula Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
olivopontocerebellar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the olivopontocerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
axillary apocrine gland hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the axillary apocrine gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Dental Enamel Hypoplasia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Dental Enamel Hypoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
testis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the testis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
tongue hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the tongue hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
genital tubercle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the genital tubercle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lymphoid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lymphoid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palatine bone horizontal plate hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thyroid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hindbrain hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hindbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
midface hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the midface hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
intervertebral disk hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the intervertebral disk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lymph node hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lymph node hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pituitary intermediate lobe hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
temporal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iris stroma hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the iris stroma hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ischium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ischium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
oviduct hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the oviduct hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spleen hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
radius hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the radius hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
otic vesicle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the otic vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
malleus hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the malleus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
maxilla hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the maxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterine cervix hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterine cervix hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
adrenal gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the adrenal gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palatal shelf hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palatal shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricle myocardium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ventricle myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
leydig cell hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the leydig cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mammary gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mammary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
scrotum hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the scrotum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
diencephalon hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the diencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cochlear ganglion hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cochlear ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
frontal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the frontal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
head mesenchyme hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the head mesenchyme hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
myometrium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the myometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
papillary muscle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the papillary muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cerebellum vermis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sebaceous gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
premaxilla hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the premaxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
atrium myocardium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrium myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
female preputial gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epididymis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the epididymis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
parathyroid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the parathyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
olfactory bulb hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the olfactory bulb hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aorta hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
heart hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the heart hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ethmoturbinate hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ethmoturbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hyoid bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hyoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pituitary gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pituitary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
parietal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the parietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
axial mesoderm hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the axial mesoderm hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mesangial cell hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mesangial cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
liver hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palatine bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palatine bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
gonial bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the gonial bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ear lobe hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ear lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
conotruncal ridge hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the conotruncal ridge hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
adenohypophysis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the adenohypophysis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
alisphenoid bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the alisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vascular smooth muscle cell hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vascular smooth muscle cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hypaxial muscle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hypaxial muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
basisphenoid bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the basisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pterygoid bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pterygoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
endometrium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the endometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vagina hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vagina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dorsal root ganglion hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dorsal root ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aorta tubular hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aorta tubular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
metacarpal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the metacarpal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
axial skeleton hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the axial skeleton hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
submandibular gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the submandibular gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
myocardial trabeculae hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the myocardial trabeculae hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vas deferens hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vas deferens hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cerebellum hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cerebellum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sinus venosus hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sinus venosus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney medulla hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney medulla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pubis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pubis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ascending aorta hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ascending aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mandible hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mandible hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
midbrain hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the midbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
nasal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the nasal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney cortex hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney cortex hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
maxillary shelf hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the maxillary shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
rathke's pouch hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the rathke's pouch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
clavicle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the clavicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sertoli cell hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sertoli cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eyelid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eyelid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
turbinate hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the turbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vertebral body hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vertebral body hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary trunk hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary trunk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreatic acinar hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vestibular ganglion hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vestibular ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
clitoris hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the clitoris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
placental labyrinth hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the placental labyrinth hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ovary hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
exocrine pancreas hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ureter hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ureter hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
glossopharyngeal nerve hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the glossopharyngeal nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
telencephalon hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the telencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
forebrain hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the forebrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
scapular bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the scapular bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreatic islet hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreatic islet hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
seminal vesicle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharynx hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharynx hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
myocardium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
trachea hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the trachea hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thymus cortex hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thymus cortex hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palate bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palate bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricular myocardium compact layer hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ventricular myocardium compact layer hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
inner ear hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the inner ear hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vomer bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vomer bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
optic nerve hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
meibomian gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the meibomian gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricular hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ventricular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
interparietal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the interparietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterus hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
esophagus hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the esophagus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
stomach hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the stomach hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lateral prostate gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lateral prostate gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
atrium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
bulbourethral gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the bulbourethral gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
philtrum hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the philtrum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
presphenoid bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the presphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
heart right ventricle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the heart right ventricle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
urinary bladder hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the urinary bladder hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
trabecula carnea hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the trabecula carnea hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |