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Results for "restrictive dermopathy, lethal": 4 genes, 136 gene sets

Name

CMR1A Gene

cardiomyopathy, restrictive 1A (autosomal dominant)

RCM2 Gene

cardiomyopathy, familial restrictive, 2

CMR2A Gene

cardiomyopathy, restrictive 2A (autosomal recessive)

CMR3A Gene

cardiomyopathy, restrictive 3A (X-linked)

restrictive dermopathy, lethal Gene Set

From OMIM Gene-Disease Associations

genes associated with the restrictive dermopathy, lethal phenotype from the curated OMIM Gene-Disease Associations dataset.

Restrictive dermopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Restrictive dermopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Restrictive dermopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Restrictive dermopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Nephrogenic Fibrosing Dermopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephrogenic Fibrosing Dermopathy from the curated CTD Gene-Disease Associations dataset.

dermopathy Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dermopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Nephrogenic Fibrosing Dermopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Nephrogenic Fibrosing Dermopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Nephrogenic Fibrosing Dermopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Nephrogenic Fibrosing Dermopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial restrictive cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, restrictive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, restrictive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, Restrictive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Restrictive from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.

restrictive cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease restrictive cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cardiomyopathy, hypertrophic; cardiomyopathy, restrictive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; cardiomyopathy, restrictive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

desmin-associated restrictive cardiomyopathy. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease desmin-associated restrictive cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

restrictive Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term restrictive in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

restrictive behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nonprogressive restrictive external ophthalmoplegia Gene Set

From HPO Gene-Disease Associations

genes associated with the nonprogressive restrictive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive external ophthalmoplegia Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive respiratory insufficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive respiratory insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive heart failure Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive heart failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restrictive lung disease Gene Set

From HPO Gene-Disease Associations

genes associated with the restrictive lung disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cardiomyopathy, Restrictive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cardiomyopathy, Restrictive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cardiomyopathy, familial restrictive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial restrictive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial restrictive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Restrictive Cardiomyopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Restrictive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Restrictive Lung Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Restrictive Lung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Restrictive Cardiomyopathy (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Restrictive Cardiomyopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Other Restrictive Cardiomyopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Other Restrictive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Nonprogressive Restrictive External Ophthalmoplegia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Nonprogressive Restrictive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Airway Disease Restrictive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Airway Disease Restrictive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Restrictive Ventilatory Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Restrictive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Restrictive Behavior Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Restrictive Behavior in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Restrictive Deficit On Pulmonary Function Testing Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Restrictive Deficit On Pulmonary Function Testing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Restrictive External Ophthalmoplegia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Restrictive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Restrictive cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Restrictive cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Restrictive cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Restrictive cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Restrictive cardiomyopathy 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Restrictive cardiomyopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Restrictive cardiomyopathy 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Restrictive cardiomyopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Restrictive cardiomyopathy 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Restrictive cardiomyopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Familial restrictive cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial restrictive cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Restrictive cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Restrictive cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta, recessive perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta, recessive perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contracture syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amish lethal microcephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amish lethal microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Popliteal pterygium syndrome lethal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contractural syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal arthrogryposis with anterior horn cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contracture syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa, lethal acantholytic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa, lethal acantholytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Clostridium difficile lethal toxin B Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Clostridium difficile lethal toxin B from the curated CTD Gene-Chemical Interactions dataset.

Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease Associations dataset.

Tight skin contracture syndrome, lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tight skin contracture syndrome, lethal from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contracture Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.

Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platyspondylic Lethal Skeletal Dysplasia, Torrance Type from the curated CTD Gene-Disease Associations dataset.

Finnish lethal neonatal metabolic syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Finnish lethal neonatal metabolic syndrome from the curated CTD Gene-Disease Associations dataset.

Amish lethal microcephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amish lethal microcephaly from the curated CTD Gene-Disease Associations dataset.

Lethal congenital contracture syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contractural Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contractural Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Epidermolysis bullosa, lethal acantholytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis bullosa, lethal acantholytic from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease of Heart, Lethal Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Perinatal Lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Perinatal Lethal from the curated CTD Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.

lethal midline granuloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease lethal midline granuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lethal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term lethal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

lethal skeletal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal skeletal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lethal short-limbed short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal short-limbed short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Granuloma, Lethal Midline Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Granuloma, Lethal Midline phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lethal giant larvae (Lgl)-like, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal giant larvae (Lgl)-like, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lethal(2) giant larvae protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal(2) giant larvae protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lethal giant larvae homologue 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal giant larvae homologue 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein male-specific lethal-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein male-specific lethal-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

popliteal pterygium syndrome 2, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the popliteal pterygium syndrome 2, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple pterygium syndrome, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, lethal, with anterior horn cell disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis, lethal, with anterior horn cell disease phenotype from the curated OMIM Gene-Disease Associations dataset.

epidermolysis bullosa, lethal acantholytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa, lethal acantholytic phenotype from the curated OMIM Gene-Disease Associations dataset.

glycogen storage disease of heart, lethal congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the glycogen storage disease of heart, lethal congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

gaucher disease, perinatal lethal Gene Set

From OMIM Gene-Disease Associations

genes associated with the gaucher disease, perinatal lethal phenotype from the curated OMIM Gene-Disease Associations dataset.

cpt ii deficiency, lethal neonatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the cpt ii deficiency, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contractural syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contractural syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contractural syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contractural syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Lethal Skeletal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Skeletal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Congenital Contractural Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Congenital Contractural Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Pterygium Syndrome, Lethal Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Pterygium Syndrome, Lethal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Platyspondylic Lethal Skeletal Dysplasia, Torrance Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Congenital Contracture Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Congenital Contracture Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Short-Limbed Short Stature Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Short-Limbed Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Tight Skin Contracture Syndrome (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Tight Skin Contracture Syndrome (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Gaucher Disease, Perinatal Lethal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Gaucher Disease, Perinatal Lethal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal midline granuloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal midline granuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal congenital contracture syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital glycogen storage disease of heart Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal congenital glycogen storage disease of heart in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal congenital contracture syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal congenital contracture syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal congenital contracture syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Gaucher's disease perinatal lethal Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Gaucher's disease perinatal lethal in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lethal congenital contracture syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal short-limb skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal short-limb skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal tight skin contracture syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal tight skin contracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Gaucher disease perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Gaucher disease perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal congenital contracture syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal congenital contracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal arthrogryposis-anterior horn cell disease syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal arthrogryposis-anterior horn cell disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal congenital contractural syndrome Finnish Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal congenital contractural syndrome Finnish phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal congenital glycogen storage disease of heart Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal congenital glycogen storage disease of heart phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Perinatal lethal hypophosphatasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Perinatal lethal hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal acantholytic epidermolysis bullosa Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal acantholytic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Amish lethal microcephaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Amish lethal microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal Kniest-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal Kniest-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal osteosclerotic bone dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal osteosclerotic bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal Encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal polymalformative syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal polymalformative syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal occipital encephalocele-skeletal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal occipital encephalocele-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Complex lethal osteochondrodysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Complex lethal osteochondrodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

NEK9-related lethal skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the NEK9-related lethal skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.