Myotubular Myopathy With Abnormal Genital Development

Clear Filter

Results for "Myotubular Myopathy With Abnormal Genital Development": 1001 gene sets

Name
Myotubular Myopathy With Abnormal Genital Development Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotubular Myopathy With Abnormal Genital Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe X-linked myotubular myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
mild myotubular myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mild myotubular myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myotubular myopathy, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the myotubular myopathy, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
Autosomal Dominant Myotubular Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Myotubular Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myotubular (Centronuclear) Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myotubular (Centronuclear) Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe X-linked myotubular myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe X-linked myotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
abnormal genital system morphology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal genital system morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal genital tubercle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal genital tubercle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal genital tubercle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal genital tubercle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sperm migration in female genital tract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From 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.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chondrodysplasia, acromesomelic, with genital anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chondrodysplasia, acromesomelic, with genital anomalies from the curated CTD Gene-Disease Associations dataset.
Genital Neoplasms, Female Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genital Neoplasms, Female from the curated CTD Gene-Disease Associations dataset.
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set From 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.
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.
Genital Diseases, Male Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Male from the curated CTD Gene-Disease Associations dataset.
ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.
Genital Diseases, Female Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Female from the curated CTD Gene-Disease Associations dataset.
genital herpes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease genital herpes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
prolapse of female genital organ Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prolapse of female genital organ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydia infections; genital diseases, female Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydia infections; genital diseases, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genital herpes; herpes genitalis Gene Set From GAD Gene-Disease Associations genes associated with the disease genital herpes; herpes genitalis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydia infections; genital diseases, female; infertility, female; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydia infections; genital diseases, female; infertility, female; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genital herpes; herpes genitalis; stomatitis, herpetic Gene Set From GAD Gene-Disease Associations genes associated with the disease genital herpes; herpes genitalis; stomatitis, herpetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genital diseases, female Gene Set From GAD Gene-Disease Associations genes associated with the disease genital diseases, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genital neoplasms, female Gene Set From GAD Gene-Disease Associations genes associated with the disease genital neoplasms, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
genital Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term genital in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Puberty onset (genital enlargement) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Puberty onset (genital enlargement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
prolapse of female genital organ Gene Set From GWASdb SNP-Disease Associations genes associated with the disease prolapse of female genital organ in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
genital neoplasm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the genital neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the genital system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
genital hernia Gene Set From HPO Gene-Disease Associations genes associated with the genital hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
genital tract atresia Gene Set From HPO Gene-Disease Associations genes associated with the genital tract atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the genital system Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the genital system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
genital neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the genital neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
external genital hypoplasia Gene Set From 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.
genital ulcers Gene Set From HPO Gene-Disease Associations genes associated with the genital ulcers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Genital Neoplasms, Male Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Neoplasms, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Genital Neoplasms, Female Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Neoplasms, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Genital Diseases, Male Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Diseases, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Genital Diseases, Female Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Diseases, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
genital hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the genital hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
genital tubercle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the genital tubercle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
chrondrodysplasia, acromesomelic, with genital anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the chrondrodysplasia, acromesomelic, with genital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
skeletal defects, genital hypoplasia, and mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set From OMIM Gene-Disease Associations genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
antley-bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From OMIM Gene-Disease Associations genes associated with the antley-bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
internal male genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
external male genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue external male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
internal female genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
external female genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue external female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
internal male genital organ Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal male genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
internal female genital organ Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal female genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
genital chamber Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue genital chamber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
external male genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
internal female genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
genital mucosa Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue genital mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
genital primordium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue genital primordium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
genital pore Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue genital pore in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
internal male genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
external female genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Genital Herpes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Herpes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Genital Herpes Simplex Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Genital Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chlamydia Trachomatis Infection Of Genital Structure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chlamydia Trachomatis Infection Of Genital Structure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genital Ulcers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Ulcers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Branchio-Skeleto-Genital Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Branchio-Skeleto-Genital Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genital Lichen Planus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Lichen Planus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genital Lichen Sclerosus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Lichen Sclerosus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genital Infantilism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Infantilism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Facio-Digito-Genital Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Facio-Digito-Genital Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genital Tuberculosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Tuberculosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Genital Vulvovaginal Candidiasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Genital Vulvovaginal Candidiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Genital System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Genital System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
External Genital Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype External Genital Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Genital Hernia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genital Hernia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Genital Edema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genital Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Genital Edema, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Genital Edema, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
impaired sperm migration in female genital tract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
genital tubercle hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the genital tubercle hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hand-foot-genital syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease hand-foot-genital syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Genital herpes Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Genital herpes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hand-foot-genital syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hand-foot-genital syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Prolapse of female genital organ Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Prolapse of female genital organ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Agenesis of corpus callosum, cardiac, ocular, and genital syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Agenesis of corpus callosum, cardiac, ocular, and genital syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Internal female genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Internal male genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
External female genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue External female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
External male genital organ Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue External male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Internal male genital organ Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal male genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Internal female genital organ Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal female genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Internal female genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Internal male genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
External male genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
External female genital organ Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Genital mucosa Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Genital mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Genital pore Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Genital pore in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Genital chamber Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Genital chamber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Genital primordium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Genital primordium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Hand-foot-genital syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand-foot-genital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Puberty onset (genital enlargement) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Puberty onset (genital enlargement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
cardiac neural crest cell development involved in heart development Gene Set From GO Biological Process Annotations 2015 genes participating in the cardiac neural crest cell development involved in heart development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of vasculature development involved in avascular cornea development in camera-type eye Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of vasculature development involved in avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset.
cardiac neural crest cell development involved in heart development Gene Set From GO Biological Process Annotations 2023 genes participating in the cardiac neural crest cell development involved in heart development biological process from the curated GO Biological Process Annotations 2023 dataset.
Mammary gland development pathway Embryonic development Stage 1 of 4 Gene Set From WikiPathways Pathways 2024 proteins participating in the Mammary gland development pathway Embryonic development Stage 1 of 4 pathway from the WikiPathways Pathways 2024 dataset.
negative regulation of vasculature development involved in avascular cornea development in camera-type eye Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of vasculature development involved in avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset.
cardiac neural crest cell development involved in heart development Gene Set From GO Biological Process Annotations 2025 genes participating in the cardiac neural crest cell development involved in heart development biological process from the curated GO Biological Process Annotations 2025 dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bethlem myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bethlem myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myofibrillar myopathy, ZASP-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, ZASP-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, centronuclear Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 3, autosomal dominant or recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, reducing body, X-linked, early-onset, severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, centronuclear, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, myosin storage Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, myosin storage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with cores Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Minicore myopathy with external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Minicore myopathy with external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Visceral myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Visceral myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Native American myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Native American myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nonaka myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nonaka myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, tubular aggregate, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, tubular aggregate, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myofibrillar myopathy, filamin C-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy, filamin C-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy with lactic acidosis, hereditary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy with lactic acidosis, hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with excess of thin myofilaments Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal myopathy Markesbery-Griggs type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, with excess of muscle spindles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary myopathy with early respiratory failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked myopathy with postural muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutral lipid storage disease with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, compton-north Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked dominant scapuloperoneal myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked dominant scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myofibrillar myopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myofibrillar myopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brody myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brody myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nemaline myopathy 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nemaline myopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, centronuclear, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, centronuclear, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, reducing body, X-linked, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miyoshi myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Miyoshi myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy with tubular aggregates Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy with tubular aggregates phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myopathy with fiber type disproportion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYOPATHY, CENTRONUCLEAR, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, 2 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CENTRONUCLEAR, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, 1 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Central Core Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Central Core from the curated CTD Gene-Disease Associations dataset.
Bethlem myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bethlem myopathy from the curated CTD Gene-Disease Associations dataset.
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.
Myopathy, Distal, with Anterior Tibial Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.
Miyoshi myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miyoshi myopathy from the curated CTD Gene-Disease Associations dataset.
Welander distal myopathy, Swedish type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, MYOFIBRILLAR, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 1 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, MYOFIBRILLAR, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 4 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, MYOFIBRILLAR, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, MYOFIBRILLAR, 6 from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 6 from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 1 from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 5 from the curated CTD Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.
Scapuloperoneal Myopathy, X-Linked Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant from the curated CTD Gene-Disease Associations dataset.
Myopathy, Hyaline Body, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Hyaline Body, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, Compton-North Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL MYOPATHY, MYH7-RELATED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL MYOPATHY, MYH7-RELATED from the curated CTD Gene-Disease Associations dataset.
Neutral Lipid Storage Disease with Myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset.
Distal myopathy, Nonaka type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Hereditary Myopathy with Early Respiratory Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, SPHEROID BODY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, SPHEROID BODY from the curated CTD Gene-Disease Associations dataset.
Minicore Myopathy with External Ophthalmoplegia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Minicore Myopathy with External Ophthalmoplegia from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, with Excessive Autophagy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, with Excessive Autophagy from the curated CTD Gene-Disease Associations dataset.
Myopathy with Lactic Acidosis, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CENTRONUCLEAR, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CENTRONUCLEAR, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Myopathy, Myosin Storage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Myosin Storage from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 3 from the curated CTD Gene-Disease Associations dataset.
Nemaline myopathy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline myopathy 4 from the curated CTD Gene-Disease Associations dataset.
Nemaline Myopathy 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline Myopathy 2 from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy 3, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Inclusion body myopathy autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion body myopathy autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Brody myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brody myopathy from the curated CTD Gene-Disease Associations dataset.
Nemaline Myopathy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nemaline Myopathy 7 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.
mitochondrial myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease mitochondrial myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
brody myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease brody myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bethlem myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bethlem myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
nemaline myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease nemaline myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
central core myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease central core myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital structural myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital structural myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
centronuclear myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease centronuclear myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy of extraocular muscle Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease myopathy of extraocular muscle from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
myopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease myopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
congenital structural myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
central core myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central core myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
brody myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brody myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myopathy of extraocular muscle Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bethlem myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bethlem myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
x-linked myopathy with excessive autophagy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease x-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
nemaline myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nemaline myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adult onset multi/minicore myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease adult onset multi/minicore myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variable myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease variable myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inherited myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease inherited myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mitochondrial myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mitochondrial myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nemaline myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease nemaline myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy, idiopathic inflammatory Gene Set From GAD Gene-Disease Associations genes associated with the disease myopathy, idiopathic inflammatory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term myopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
myopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease myopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
scapuloperoneal myopathy Gene Set From HPO Gene-Disease Associations genes associated with the scapuloperoneal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myofibrillar myopathy Gene Set From HPO Gene-Disease Associations genes associated with the myofibrillar myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mitochondrial myopathy Gene Set From HPO Gene-Disease Associations genes associated with the mitochondrial myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skeletal myopathy Gene Set From HPO Gene-Disease Associations genes associated with the skeletal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myopathy Gene Set From HPO Gene-Disease Associations genes associated with the myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
minicore (multicore) myopathy Gene Set From HPO Gene-Disease Associations genes associated with the minicore (multicore) myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
myopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
nemaline myopathy 6, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, spheroid body Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, spheroid body phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy with extrapyramidal signs Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy with extrapyramidal signs phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, early-onset, with fatal cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
centronuclear myopathy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the centronuclear myopathy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myosin storage Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myosin storage phenotype from the curated OMIM Gene-Disease Associations dataset.
native american myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the native american myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, x-linked, with postural muscle atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 1, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 1, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, tubular aggregate Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, tubular aggregate phenotype from the curated OMIM Gene-Disease Associations dataset.
epiphyseal dysplasia, multiple, with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set From OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 8, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 8, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 4, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
brody myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the brody myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neutral lipid storage disease with myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the neutral lipid storage disease with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, actin, congenital, with cores Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, actin, congenital, with cores phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
?myopathy, congenital, compton-north Gene Set From OMIM Gene-Disease Associations genes associated with the ?myopathy, congenital, compton-north phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy with lactic acidosis, hereditary Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy with lactic acidosis, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 5, amish type Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 5, amish type phenotype from the curated OMIM Gene-Disease Associations dataset.
?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital myopathy with excess of muscle spindles Gene Set From OMIM Gene-Disease Associations genes associated with the congenital myopathy with excess of muscle spindles phenotype from the curated OMIM Gene-Disease Associations dataset.
welander distal myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
bethlem myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the bethlem myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, proximal, with early respiratory muscle involvement Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
laing distal myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set From OMIM Gene-Disease Associations genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?myopathy, tubular aggregate, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?myopathy, tubular aggregate, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal myopathy, x-linked dominant Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal myopathy, x-linked dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 7, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 7, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
mitochondrial myopathy and sideroblastic anemia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the mitochondrial myopathy and sideroblastic anemia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 3, autosomal dominant or recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 3, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
minicore myopathy with external ophthalmoplegia Gene Set From OMIM Gene-Disease Associations genes associated with the minicore myopathy with external ophthalmoplegia phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, with anterior tibial onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.
cap myopathy 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cap myopathy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cap myopathy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cap myopathy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{centronuclear myopathy, autosomal, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {centronuclear myopathy, autosomal, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion phenotype from the curated OMIM Gene-Disease Associations dataset.
inclusion body myopathy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the inclusion body myopathy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 9 Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, centronuclear Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, centronuclear phenotype from the curated OMIM Gene-Disease Associations dataset.
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, severe early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 2, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy due to cpt ii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
nonaka myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the nonaka myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, tateyama type Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset.
visceral myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the visceral myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, actin, congenital, with excess of thin myofilaments Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated OMIM Gene-Disease Associations dataset.
nemaline myopathy 10 Gene Set From OMIM Gene-Disease Associations genes associated with the nemaline myopathy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy due to myoadenylate deaminase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease myopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Inclusion Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neutral Lipid Storage Disease With Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neutral Lipid Storage Disease With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Core Myopathy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Core Myopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Centronuclear Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Centronuclear Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Actin-Accumulation Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Actin-Accumulation Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Centronuclear Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Centronuclear Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Structural Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Structural Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intranuclear Rod Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intranuclear Rod Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myofibrillar Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myofibrillar Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nemaline Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nemaline Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonaka Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonaka Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tubular Aggregate Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tubular Aggregate Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vacuolar Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vacuolar Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zebra Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zebra Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Myopathy, Familial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Myopathy, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Miyoshi Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miyoshi Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bethlem Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bethlem Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minicore Myopathy With External Ophthalmoplegia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minicore Myopathy With External Ophthalmoplegia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multi-Core Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multi-Core Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Myopathy, X-Linked Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Myopathy, X-Linked Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sarcoid Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sarcoid Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcohol Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brody Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brody Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Axial Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Critical Illness Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Critical Illness Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Welander Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy With Focal Depletion Of Mitochondria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epiphyseal Dysplasia, Multiple, With Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing-Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing-Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Myopathy With Early Respiratory Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Myopathy With Early Respiratory Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Native American Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Native American Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngodistal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngodistal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Klhl9-Related Early-Onset Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Myopathy 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Myopathy With Abundant Macrophages Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Myopathy With Abundant Macrophages in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inclusion Body Myopathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inclusion Body Myopathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spheroid Body Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spheroid Body Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitochondrial Myopathy With Lactic Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Myopathy With Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy 1 With Or Without Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyglucosan Body Myopathy Type 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyglucosan Body Myopathy Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Samaritan Congenital Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Samaritan Congenital Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Myopathy With Myasthenic-Like Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Myopathy With Myasthenic-Like Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Desmin Related Myopathy With Mallory Body-Like Inclusions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Desmin Related Myopathy With Mallory Body-Like Inclusions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy, Tpm2-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy, Tpm2-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cap Myopathy, Tpm3-Related (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cap Myopathy, Tpm3-Related (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
myopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the myopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Nemaline myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Nemaline myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Mitochondrial myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Mitochondrial myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myofibrillar myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myofibrillar myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
GNE myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease GNE myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital structural myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital structural myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Centronuclear myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Centronuclear myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 4A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 4A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myofibrillar myopathy 9 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myofibrillar myopathy 9 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Native American myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Native American myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hyaline body myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyaline body myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal myopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Brody myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Brody myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 1B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Nemaline myopathy 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Nemaline myopathy 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital myopathy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital myopathy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Centronuclear myopathy X-linked Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Centronuclear myopathy X-linked from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Myopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with Paget disease of bone and frontotemporal dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital structural myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
GNE myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease GNE myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy X-linked Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy X-linked in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngodistal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngodistal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fatal infantile hypertonic myofibrillar myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy with rimmed vacuoles Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
COX deficiency, benign infantile mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease COX deficiency, benign infantile mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked myopathy with excessive autophagy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bethlem myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bethlem myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy with anterior tibial onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Compton-North congenital myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Compton-North congenital myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Scapuloperoneal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 6 with fiber-type disproportion Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 6 with fiber-type disproportion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Brody myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brody myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cylindrical spirals myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cylindrical spirals myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 4A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 4A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy with extrapyramidal signs Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy with extrapyramidal signs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive centronuclear myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive centronuclear myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Isolated mitochondrial myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Isolated mitochondrial myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 5A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 5A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Native American myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Native American myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Centronuclear myopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Centronuclear myopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oculopharyngodistal myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oculopharyngodistal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myofibrillar myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myofibrillar myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy of extraocular muscle Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myopathy of extraocular muscle in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 22A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 22A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tubular aggregate myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tubular aggregate myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nemaline myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nemaline myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital myopathy 22B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital myopathy 22B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive hyaline body myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive hyaline body myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in F Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in F phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SELENON-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SELENON-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN4A-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN4A-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GNE myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GNE myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sarcotubular myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sarcotubular myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inclusion body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TPM3-related core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM3-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nemaline myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nemaline myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Central core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Central core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital multicore myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital multicore myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RYR1-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RYR1-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYH7-related skeletal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH7-related skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myosin storage myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myosin storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visceral myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visceral myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Desmin-related myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Desmin-related myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bethlem myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bethlem myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Collagen 6-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Collagen 6-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Batten-Turner congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Batten-Turner congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Brody myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Brody myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inborn mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inborn mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Actin accumulation myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Actin accumulation myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy 2b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 2b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy 2c Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 2c phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive scapulohumeroperoneal distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital myopathy 10b Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital myopathy 10b phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MEGF10-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MEGF10-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYPN-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYPN-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neutral lipid storage myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral lipid storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Welander distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal infantile hypertonic myofibrillar myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal infantile hypertonic myofibrillar myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapuloperoneal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability and myopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability and myopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TTN-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TTN-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in POMG Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in POMG phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bailey-Bloch congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bailey-Bloch congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiminicore myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiminicore myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Miyoshi myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Miyoshi myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in PO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in PO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Compton-North congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Compton-North congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy due to lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion-body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion-body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Polyglucosan body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Polyglucosan body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HNRNPDL-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HNRNPDL-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Axial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Axial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SGCG-related congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SGCG-related congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy-lactic acidosis-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-lactic acidosis-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CAP-congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CAP-congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ACTA1 gene related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTA1 gene related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy due to calsequestrin and SERCA1 protein overload Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy due to calsequestrin and SERCA1 protein overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital nonprogressive myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nonprogressive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyaline body myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyaline body myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TPM2-related cap myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM2-related cap myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYH2-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH2-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inclusion body myopathy and brain white matter abnormalities Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inclusion body myopathy and brain white matter abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital structural myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital structural myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood-onset autosomal recessive myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Skeletal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TPM2-related myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TPM2-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive centronuclear myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic inflammatory myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
COL6A2-related core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the COL6A2-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Finnish upper limb-onset distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SPEG-related congenital myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SPEG-related congenital myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
IDUA-related core myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the IDUA-related core myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oculopharyngodistal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oculopharyngodistal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Simvastatin-induced myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Simvastatin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Atorvastatin-induced myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Atorvastatin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Statin-induced myopathy (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Statin-induced myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Statin-induced myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic inflammatory myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic inflammatory myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
abnormal urogenital development Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormal ear development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal thyroid gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lens development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lens development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal otic vesicle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal digestive system development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal brain development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal meibomian gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vagina development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vagina development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mesendoderm development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mesendoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal metanephric ureteric bud development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal metanephric ureteric bud development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal endometrial gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrial gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal muscle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal corneal stroma development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal corneal stroma development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal adipose tissue development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal adipose tissue development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vertebrae development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebrae development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hippocampus development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vascular development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tail development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tail development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vascular smooth muscle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular smooth muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neural tube morphology/development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neural tube morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal intervertebral disk development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal intervertebral disk development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lens vesicle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lens vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellum development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal placenta development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal adenohypophysis development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal adenohypophysis development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal rib development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal rib development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lung alveolus development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lung alveolus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal digit development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal digit development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ovary development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mammary gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pallium development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pallium development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal prostate gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal forebrain development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal forebrain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal uterus development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal uterus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal retinal development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal testis development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal testis development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile duct development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal artery development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal artery development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal adrenal gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal adrenal gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lacrimal gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal somite development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal somite development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hair follicle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth root development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth root development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal heart development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal heart development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neurohypophysis development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neurohypophysis development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal seminal vesicle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal seminal vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal limb development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal limb development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal endocrine pancreas development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal endocrine pancreas development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal otic capsule development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal otic capsule development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal primary palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal primary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal head development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal head development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal myotome development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal myotome development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vein development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vein development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal olfactory bulb development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hepatobiliary system development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatobiliary system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pharyngeal arch development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal preimplantation embryo development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal preimplantation embryo development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal eye muscle development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal craniofacial development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal craniofacial development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal thymus development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal thymus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vascular endothelial cell development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal rathke's pouch development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal rathke's pouch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal tooth development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal kidney medulla development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney medulla development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pluripotent precursor cell morphology/development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pluripotent precursor cell morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ureter development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ureter development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hematopoietic system morphology/development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hematopoietic system morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mesenchymal cell proliferation involved in lung development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mesenchymal cell proliferation involved in lung development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal endoderm development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal endoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal inner ear development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal eyelid development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal eyelid development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pancreas development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal kidney development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal myeloblast morphology/development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal myeloblast morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal blood cell morphology/development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal blood cell morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal nervous system development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal nervous system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mesoderm development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mesoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal respiratory system development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal respiratory system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lung development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lung development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic arch development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal eye development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal eye development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal telencephalon development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal telencephalon development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal dermomyotome development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal dermomyotome development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal midbrain-hindbrain boundary development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal midbrain-hindbrain boundary development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal triploblastic development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal triploblastic development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal intestine development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sertoli cell development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sertoli cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vertebral arch development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mammary gland embryonic development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland embryonic development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lung-associated mesenchyme development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lung-associated mesenchyme development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal reproductive system development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal reproductive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cartilage development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cartilage development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lymph organ development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph organ development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cardiovascular development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cardiovascular development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bone marrow development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cecum development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cecum development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal diaphragm development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal diaphragm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal nipple development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal nipple development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear hair cell development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vestibular hair cell development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal extraembryonic mesoderm development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal extraembryonic mesoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hymen development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hymen development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ectoderm development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ectoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bone marrow cell morphology/development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal esophagus development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal esophagus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal midbrain development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal midbrain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vertebral body development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral body development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal liver development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal liver development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mesenchymal cell differentiation involved in lung development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mesenchymal cell differentiation involved in lung development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skeleton development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skeleton development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal outflow tract development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal outflow tract development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal urinary system development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hindbrain development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hindbrain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal embryogenesis/ development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal embryogenesis/ development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pituitary gland development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spleen development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Abnormal Sperm Development Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Sperm Development in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abnormal lens development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lens development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal brain development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ectoderm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ectoderm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mesoderm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mesoderm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vascular development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vascular endothelial cell development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular endothelial cell development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal eye development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal craniofacial development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal craniofacial development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lung development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal esophagus development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal esophagus development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal liver development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mesendoderm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mesendoderm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal anterior head development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior head development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal heart development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal somite development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somite development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal skeleton development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skeleton development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cartilage development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cartilage development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal dermomyotome development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dermomyotome development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal germ layer development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal germ layer development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal digit development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal digit development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lens vesicle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lens vesicle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal limb development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal limb development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal embryo development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hindbrain development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hindbrain development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal otic vesicle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal placenta development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placenta development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal nervous system development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nervous system development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal otic capsule development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal otic capsule development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal eye muscle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal adenohypophysis development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adenohypophysis development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal Rathke's pouch development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Rathke's pouch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal rib development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal rib development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal digestive system development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal forebrain development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal forebrain development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal midbrain development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal midbrain development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal endoderm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endoderm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal extraembryonic mesoderm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extraembryonic mesoderm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vertebral body development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vertebral body development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal Sertoli cell development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Sertoli cell development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mesenchymal cell proliferation involved in lung development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mesenchymal cell proliferation involved in lung development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile duct development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pancreas development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ear development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ear development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pituitary gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pituitary gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cecum development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cecum development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal head development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal head development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal myotome development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal myotome development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal kidney development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spleen development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal eyelid development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eyelid development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal corneal stroma development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal stroma development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hair follicle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cochlear hair cell development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary palate development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hippocampus development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hippocampus development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal skin development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skin development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal uterus development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal uterus development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal uterine epithelium development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal uterine epithelium development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vertebrae development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vertebrae development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ureter development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ureter development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal telencephalon development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal telencephalon development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal thymus development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thymus development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal midbrain-hindbrain boundary development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal midbrain-hindbrain boundary development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellum development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mammary gland embryonic development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland embryonic development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cardiac outflow tract development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cardiac outflow tract development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bulbourethral gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bulbourethral gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal endocrine pancreas development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endocrine pancreas development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vertebral arch development Gene Set From 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.
abnormal olfactory bulb development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal olfactory bulb development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal testis development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal testis development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal prostate gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prostate gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal seminal vesicle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal seminal vesicle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal kidney medulla development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney medulla development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal thyroid gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal parathyroid gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal parathyroid gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal metanephric ureteric bud development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal metanephric ureteric bud development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal neurohypophysis development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neurohypophysis development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal periderm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal periderm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal preimplantation embryo development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal preimplantation embryo development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bone marrow cell morphology/development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone marrow cell morphology/development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal adrenal gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adrenal gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal reproductive system development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal reproductive system development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal diaphragm development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal diaphragm development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal intervertebral disk development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intervertebral disk development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hematopoietic system morphology/development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hematopoietic system morphology/development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tail development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tail development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mammary gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vagina development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vagina development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pallium development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pallium development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal myeloblast morphology/development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal myeloblast morphology/development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal respiratory system development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal respiratory system development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal muscle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal muscle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bone marrow development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone marrow development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal blood cell morphology/development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood cell morphology/development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal dentin development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dentin development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal enamel development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enamel development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cardiovascular development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cardiovascular development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lymph organ development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymph organ development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal Meibomian gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Meibomian gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal palate development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal palate development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal mesenchymal cell differentiation involved in lung development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mesenchymal cell differentiation involved in lung development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal face development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal face development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal endometrial gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endometrial gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal retina development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal retina development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal nipple development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nipple development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal artery development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal artery development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vein development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vein development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal submandibular gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal submandibular gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ovary development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lung alveolus development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung alveolus development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lung-associated mesenchyme development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung-associated mesenchyme development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal urinary system development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urinary system development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vestibular hair cell development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal tooth root development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tooth root development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic arch development Gene Set From 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.
abnormal adipose tissue development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal adipose tissue development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pharyngeal arch development Gene Set From 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.
abnormal trachea development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal trachea development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hepatobiliary system development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatobiliary system development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal intestine development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestine development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial cartilage development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial cartilage development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vascular smooth muscle development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular smooth muscle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lacrimal gland development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal inner ear development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner ear development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal forebrain development Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal forebrain development phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal midbrain development Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal midbrain development phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal embryo development Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal embryo development phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal hindbrain development Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal hindbrain development phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal placenta development Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal placenta development phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
il12 and stat4 dependent signaling pathway in th1 development Gene Set From Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.
hop pathway in cardiac development Gene Set From Biocarta Pathways proteins participating in the hop pathway in cardiac development pathway from the Biocarta Pathways dataset.
lissencephaly gene (lis1) in neuronal migration and development Gene Set From Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.
melanocyte development and pigmentation pathway Gene Set From Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.
Child Development Disorders, Pervasive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Child Development Disorders, Pervasive from the curated CTD Gene-Disease Associations dataset.
46, XY Disorders of Sex Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46, XY Disorders of Sex Development from the curated CTD Gene-Disease Associations dataset.
Language Development Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Language Development Disorders from the curated CTD Gene-Disease Associations dataset.
46, XX Disorders of Sex Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46, XX Disorders of Sex Development from the curated CTD Gene-Disease Associations dataset.
Malformations of Cortical Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Malformations of Cortical Development from the curated CTD Gene-Disease Associations dataset.
Disorders of Sex Development Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disorders of Sex Development from the curated CTD Gene-Disease Associations dataset.
bone development disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone development disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bone development disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bone development disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mental development Gene Set From GAD Gene-Disease Associations genes associated with the disease mental development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased development of adult t-cell leukemia/lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease increased development of adult t-cell leukemia/lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malformations of cortical development Gene Set From GAD Gene-Disease Associations genes associated with the disease malformations of cortical development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haptoglobin development Gene Set From GAD Gene-Disease Associations genes associated with the disease haptoglobin development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
development of coronary artery lesions Gene Set From GAD Gene-Disease Associations genes associated with the disease development of coronary artery lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
language development disorders; mental retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease language development disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary tooth development Gene Set From GAD Gene-Disease Associations genes associated with the disease primary tooth development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nephropathy development Gene Set From GAD Gene-Disease Associations genes associated with the disease nephropathy development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast cancer development Gene Set From GAD Gene-Disease Associations genes associated with the disease breast cancer development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene Set From GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertriglyceridemia and the development of fatty liver Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertriglyceridemia and the development of fatty liver in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
language development disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease language development disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease 46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
midbrain-hindbrain boundary maturation during brain development Gene Set From GO Biological Process Annotations 2015 genes participating in the midbrain-hindbrain boundary maturation during brain development biological process from the curated GO Biological Process Annotations 2015 dataset.
vagina development Gene Set From GO Biological Process Annotations 2015 genes participating in the vagina development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of anterior head development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of anterior head development biological process from the curated GO Biological Process Annotations 2015 dataset.
cochlear nucleus development Gene Set From GO Biological Process Annotations 2015 genes participating in the cochlear nucleus development biological process from the curated GO Biological Process Annotations 2015 dataset.
optic nerve development Gene Set From GO Biological Process Annotations 2015 genes participating in the optic nerve development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal cortex development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal cortex development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of neuron projection development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of neuron projection development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellum development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellum development biological process from the curated GO Biological Process Annotations 2015 dataset.
dorsal aorta development Gene Set From GO Biological Process Annotations 2015 genes participating in the dorsal aorta development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of dendritic spine development Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of dendritic spine development biological process from the curated GO Biological Process Annotations 2015 dataset.
astrocyte development Gene Set From GO Biological Process Annotations 2015 genes participating in the astrocyte development biological process from the curated GO Biological Process Annotations 2015 dataset.
trachea development Gene Set From GO Biological Process Annotations 2015 genes participating in the trachea development biological process from the curated GO Biological Process Annotations 2015 dataset.
tendon development Gene Set From GO Biological Process Annotations 2015 genes participating in the tendon development biological process from the curated GO Biological Process Annotations 2015 dataset.
efferent axon development in a lateral line nerve Gene Set From GO Biological Process Annotations 2015 genes participating in the efferent axon development in a lateral line nerve biological process from the curated GO Biological Process Annotations 2015 dataset.
olfactory lobe development Gene Set From GO Biological Process Annotations 2015 genes participating in the olfactory lobe development biological process from the curated GO Biological Process Annotations 2015 dataset.
head development Gene Set From GO Biological Process Annotations 2015 genes participating in the head development biological process from the curated GO Biological Process Annotations 2015 dataset.
putamen development Gene Set From GO Biological Process Annotations 2015 genes participating in the putamen development biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic placenta development Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic placenta development biological process from the curated GO Biological Process Annotations 2015 dataset.
retina development in camera-type eye Gene Set From GO Biological Process Annotations 2015 genes participating in the retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset.
otic vesicle development Gene Set From GO Biological Process Annotations 2015 genes participating in the otic vesicle development biological process from the curated GO Biological Process Annotations 2015 dataset.
nerve development Gene Set From GO Biological Process Annotations 2015 genes participating in the nerve development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of apoptotic process involved in metanephric nephron tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of apoptotic process involved in metanephric nephron tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
rhombomere 3 development Gene Set From GO Biological Process Annotations 2015 genes participating in the rhombomere 3 development biological process from the curated GO Biological Process Annotations 2015 dataset.
glomerular visceral epithelial cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter involved in heart development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in heart development biological process from the curated GO Biological Process Annotations 2015 dataset.
amygdala development Gene Set From GO Biological Process Annotations 2015 genes participating in the amygdala development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric nephron tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric nephron tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cardiac muscle fiber development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cardiac muscle fiber development biological process from the curated GO Biological Process Annotations 2015 dataset.
limbic system development Gene Set From GO Biological Process Annotations 2015 genes participating in the limbic system development biological process from the curated GO Biological Process Annotations 2015 dataset.
endocardial cushion cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the endocardial cushion cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic ectodermal digestive tract development Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic ectodermal digestive tract development biological process from the curated GO Biological Process Annotations 2015 dataset.
skeletal muscle tissue development Gene Set From GO Biological Process Annotations 2015 genes participating in the skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of ovarian follicle development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of ovarian follicle development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cell differentiation involved in embryonic placenta development Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cell differentiation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations 2015 dataset.
hair follicle development Gene Set From GO Biological Process Annotations 2015 genes participating in the hair follicle development biological process from the curated GO Biological Process Annotations 2015 dataset.
canonical wnt signaling pathway involved in heart development Gene Set From GO Biological Process Annotations 2015 genes participating in the canonical wnt signaling pathway involved in heart development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of epithelial cell differentiation involved in kidney development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
dendritic spine development Gene Set From GO Biological Process Annotations 2015 genes participating in the dendritic spine development biological process from the curated GO Biological Process Annotations 2015 dataset.
cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
postganglionic parasympathetic fiber development Gene Set From GO Biological Process Annotations 2015 genes participating in the postganglionic parasympathetic fiber development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cell proliferation involved in mesonephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cell proliferation involved in mesonephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
pericardium development Gene Set From GO Biological Process Annotations 2015 genes participating in the pericardium development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cardiac muscle tissue development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cardiac muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of myotome development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of myotome development biological process from the curated GO Biological Process Annotations 2015 dataset.
face development Gene Set From GO Biological Process Annotations 2015 genes participating in the face development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
aorta development Gene Set From GO Biological Process Annotations 2015 genes participating in the aorta development biological process from the curated GO Biological Process Annotations 2015 dataset.
bronchus development Gene Set From GO Biological Process Annotations 2015 genes participating in the bronchus development biological process from the curated GO Biological Process Annotations 2015 dataset.
common bile duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the common bile duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
cell differentiation involved in metanephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the cell differentiation involved in metanephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cell proliferation involved in embryonic placenta development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cell proliferation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of embryonic development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of embryonic development biological process from the curated GO Biological Process Annotations 2015 dataset.
striated muscle cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the striated muscle cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
osteoclast development Gene Set From GO Biological Process Annotations 2015 genes participating in the osteoclast development biological process from the curated GO Biological Process Annotations 2015 dataset.
adrenal gland development Gene Set From GO Biological Process Annotations 2015 genes participating in the adrenal gland development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation involved in nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of metanephric glomerular visceral epithelial cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of metanephric glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
oculomotor nerve development Gene Set From GO Biological Process Annotations 2015 genes participating in the oculomotor nerve development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of oocyte development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of oocyte development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal system development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal system development biological process from the curated GO Biological Process Annotations 2015 dataset.
cardiac chamber development Gene Set From GO Biological Process Annotations 2015 genes participating in the cardiac chamber development biological process from the curated GO Biological Process Annotations 2015 dataset.
development of primary female sexual characteristics Gene Set From GO Biological Process Annotations 2015 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of apoptotic process involved in metanephric collecting duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of epithelial cell proliferation involved in prostate gland development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations 2015 dataset.
trigeminal nerve development Gene Set From GO Biological Process Annotations 2015 genes participating in the trigeminal nerve development biological process from the curated GO Biological Process Annotations 2015 dataset.
cardiac septum development Gene Set From GO Biological Process Annotations 2015 genes participating in the cardiac septum development biological process from the curated GO Biological Process Annotations 2015 dataset.
pronephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the pronephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
uterine epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the uterine epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
pyramidal neuron development Gene Set From GO Biological Process Annotations 2015 genes participating in the pyramidal neuron development biological process from the curated GO Biological Process Annotations 2015 dataset.
reproductive system development Gene Set From GO Biological Process Annotations 2015 genes participating in the reproductive system development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
soft palate development Gene Set From GO Biological Process Annotations 2015 genes participating in the soft palate development biological process from the curated GO Biological Process Annotations 2015 dataset.
cervix development Gene Set From GO Biological Process Annotations 2015 genes participating in the cervix development biological process from the curated GO Biological Process Annotations 2015 dataset.
respiratory tube development Gene Set From GO Biological Process Annotations 2015 genes participating in the respiratory tube development biological process from the curated GO Biological Process Annotations 2015 dataset.
rhombomere development Gene Set From GO Biological Process Annotations 2015 genes participating in the rhombomere development biological process from the curated GO Biological Process Annotations 2015 dataset.
mesonephric epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the mesonephric epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
muscle structure development Gene Set From GO Biological Process Annotations 2015 genes participating in the muscle structure development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of muscle organ development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle organ development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cardiac muscle fiber development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cardiac muscle fiber development biological process from the curated GO Biological Process Annotations 2015 dataset.
ammon gyrus development Gene Set From GO Biological Process Annotations 2015 genes participating in the ammon gyrus development biological process from the curated GO Biological Process Annotations 2015 dataset.
caudate nucleus development Gene Set From GO Biological Process Annotations 2015 genes participating in the caudate nucleus development biological process from the curated GO Biological Process Annotations 2015 dataset.
mesenchymal cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the mesenchymal cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
stromal-epithelial cell signaling involved in prostate gland development Gene Set From GO Biological Process Annotations 2015 genes participating in the stromal-epithelial cell signaling involved in prostate gland development biological process from the curated GO Biological Process Annotations 2015 dataset.
adult heart development Gene Set From GO Biological Process Annotations 2015 genes participating in the adult heart development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of mesonephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of mesonephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
mammary gland epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the mammary gland epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
bmp signaling pathway involved in heart development Gene Set From GO Biological Process Annotations 2015 genes participating in the bmp signaling pathway involved in heart development biological process from the curated GO Biological Process Annotations 2015 dataset.
axon development Gene Set From GO Biological Process Annotations 2015 genes participating in the axon development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric interstitial fibroblast development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric interstitial fibroblast development biological process from the curated GO Biological Process Annotations 2015 dataset.
thalamus development Gene Set From GO Biological Process Annotations 2015 genes participating in the thalamus development biological process from the curated GO Biological Process Annotations 2015 dataset.
mesenchymal-epithelial cell signaling involved in lung development Gene Set From GO Biological Process Annotations 2015 genes participating in the mesenchymal-epithelial cell signaling involved in lung development biological process from the curated GO Biological Process Annotations 2015 dataset.
atrioventricular node development Gene Set From GO Biological Process Annotations 2015 genes participating in the atrioventricular node development biological process from the curated GO Biological Process Annotations 2015 dataset.
blood vessel development Gene Set From GO Biological Process Annotations 2015 genes participating in the blood vessel development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of sclerotome development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of sclerotome development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of kidney development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
paramesonephric duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the paramesonephric duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
schwann cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the schwann cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal convoluted tubule segment 2 development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations 2015 dataset.
cell proliferation involved in metanephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the cell proliferation involved in metanephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric distal convoluted tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
substantia nigra development Gene Set From GO Biological Process Annotations 2015 genes participating in the substantia nigra development biological process from the curated GO Biological Process Annotations 2015 dataset.
development of primary sexual characteristics Gene Set From GO Biological Process Annotations 2015 genes participating in the development of primary sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of mesenchymal cell proliferation involved in ureter development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of mesenchymal cell proliferation involved in ureter development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
tricuspid valve development Gene Set From GO Biological Process Annotations 2015 genes participating in the tricuspid valve development biological process from the curated GO Biological Process Annotations 2015 dataset.
syncytiotrophoblast cell differentiation involved in labyrinthine layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the syncytiotrophoblast cell differentiation involved in labyrinthine layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
corpus callosum development Gene Set From GO Biological Process Annotations 2015 genes participating in the corpus callosum development biological process from the curated GO Biological Process Annotations 2015 dataset.
diaphragm development Gene Set From GO Biological Process Annotations 2015 genes participating in the diaphragm development biological process from the curated GO Biological Process Annotations 2015 dataset.
vasculature development Gene Set From GO Biological Process Annotations 2015 genes participating in the vasculature development biological process from the curated GO Biological Process Annotations 2015 dataset.
mammary gland lobule development Gene Set From GO Biological Process Annotations 2015 genes participating in the mammary gland lobule development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric glomerular mesangial cell proliferation involved in metanephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric glomerular mesangial cell proliferation involved in metanephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of cell differentiation involved in embryonic placenta development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cell differentiation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations 2015 dataset.
spongiotrophoblast layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the spongiotrophoblast layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
muscle cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the muscle cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of epithelial cell proliferation involved in prostate gland development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of muscle organ development Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of muscle organ development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of dendrite development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of dendrite development biological process from the curated GO Biological Process Annotations 2015 dataset.
limb epidermis development Gene Set From GO Biological Process Annotations 2015 genes participating in the limb epidermis development biological process from the curated GO Biological Process Annotations 2015 dataset.
venous blood vessel development Gene Set From GO Biological Process Annotations 2015 genes participating in the venous blood vessel development biological process from the curated GO Biological Process Annotations 2015 dataset.
male genitalia development Gene Set From GO Biological Process Annotations 2015 genes participating in the male genitalia development biological process from the curated GO Biological Process Annotations 2015 dataset.
vestibular nucleus development Gene Set From GO Biological Process Annotations 2015 genes participating in the vestibular nucleus development biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of mesenchymal cell apoptotic process involved in metanephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of mesenchymal cell apoptotic process involved in metanephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
pattern specification involved in kidney development Gene Set From GO Biological Process Annotations 2015 genes participating in the pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
somite development Gene Set From GO Biological Process Annotations 2015 genes participating in the somite development biological process from the curated GO Biological Process Annotations 2015 dataset.
mesenchymal-epithelial cell signaling involved in prostate gland development Gene Set From GO Biological Process Annotations 2015 genes participating in the mesenchymal-epithelial cell signaling involved in prostate gland development biological process from the curated GO Biological Process Annotations 2015 dataset.
neural tube development Gene Set From GO Biological Process Annotations 2015 genes participating in the neural tube development biological process from the curated GO Biological Process Annotations 2015 dataset.
trachea cartilage development Gene Set From GO Biological Process Annotations 2015 genes participating in the trachea cartilage development biological process from the curated GO Biological Process Annotations 2015 dataset.
cell migration involved in metanephros development Gene Set From GO Biological Process Annotations 2015 genes participating in the cell migration involved in metanephros development biological process from the curated GO Biological Process Annotations 2015 dataset.
labyrinthine layer blood vessel development Gene Set From GO Biological Process Annotations 2015 genes participating in the labyrinthine layer blood vessel development biological process from the curated GO Biological Process Annotations 2015 dataset.
forebrain development Gene Set From GO Biological Process Annotations 2015 genes participating in the forebrain development biological process from the curated GO Biological Process Annotations 2015 dataset.
development of secondary sexual characteristics Gene Set From GO Biological Process Annotations 2015 genes participating in the development of secondary sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric nephron epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric nephron epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation involved in metanephric nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
germ cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the germ cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
lateral semicircular canal development Gene Set From GO Biological Process Annotations 2015 genes participating in the lateral semicircular canal development biological process from the curated GO Biological Process Annotations 2015 dataset.
pallium development Gene Set From GO Biological Process Annotations 2015 genes participating in the pallium development biological process from the curated GO Biological Process Annotations 2015 dataset.
sinoatrial node cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the sinoatrial node cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
heart valve development Gene Set From GO Biological Process Annotations 2015 genes participating in the heart valve development biological process from the curated GO Biological Process Annotations 2015 dataset.
kidney epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the kidney epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
rhombomere 4 development Gene Set From GO Biological Process Annotations 2015 genes participating in the rhombomere 4 development biological process from the curated GO Biological Process Annotations 2015 dataset.
anatomical structure development Gene Set From GO Biological Process Annotations 2015 genes participating in the anatomical structure development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of bone development Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of bone development biological process from the curated GO Biological Process Annotations 2015 dataset.
maternal placenta development Gene Set From GO Biological Process Annotations 2015 genes participating in the maternal placenta development biological process from the curated GO Biological Process Annotations 2015 dataset.

Harmonizome 3.0

Myotubular Myopathy With Abnormal Genital Development Gene Set

Severe X-linked myotubular myopathy Gene Set

mild myotubular myopathy Gene Set

myotubular myopathy, x-linked Gene Set

Autosomal Dominant Myotubular Myopathy Gene Set

Myotubular (Centronuclear) Myopathy Gene Set

Severe X-linked myotubular myopathy Gene Set

abnormal genital system morphology Gene Set

abnormal genital system morphology Gene Set

abnormal genital tubercle morphology Gene Set

abnormal genital tubercle morphology Gene Set

abnormal sperm migration in female genital tract Gene Set

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

Chondrodysplasia, acromesomelic, with genital anomalies Gene Set

Genital Neoplasms, Female Gene Set

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set

Genital Diseases, Male Gene Set

ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set

Genital Diseases, Female Gene Set

genital herpes Gene Set

prolapse of female genital organ Gene Set

carcinoma, squamous cell; condylomata acuminata; epidermodysplasia verruciformis; squamous cell carcinoma; tumor virus infections; warts, genital Gene Set

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene Set

chlamydia infections; genital diseases, female Gene Set

genital herpes; herpes genitalis Gene Set

chlamydia infections; genital diseases, female; infertility, female; inflammation Gene Set

breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene Set

genital herpes; herpes genitalis; stomatitis, herpetic Gene Set

genital diseases, female Gene Set

genital neoplasms, female Gene Set

breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set

genital Gene Set

Puberty onset (genital enlargement) Gene Set

prolapse of female genital organ Gene Set

genital neoplasm Gene Set

abnormality of the genital system Gene Set

genital hernia Gene Set

genital tract atresia Gene Set

abnormality of the genital system Gene Set

genital neoplasm Gene Set

external genital hypoplasia Gene Set

genital ulcers Gene Set

Genital Neoplasms, Male Gene Set

Genital Neoplasms, Female Gene Set

Genital Diseases, Male Gene Set

Genital Diseases, Female Gene Set

genital hemorrhage Gene Set

genital tubercle hypoplasia Gene Set

chrondrodysplasia, acromesomelic, with genital anomalies Gene Set

skeletal defects, genital hypoplasia, and mental retardation Gene Set

antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set

antley-bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

internal male genital organ Gene Set

external male genital organ Gene Set

internal female genital organ Gene Set

external female genital organ Gene Set

internal male genital organ Gene Set

internal female genital organ Gene Set

genital chamber Gene Set

external male genital organ Gene Set

internal female genital organ Gene Set

genital mucosa Gene Set

genital primordium Gene Set

genital pore Gene Set

internal male genital organ Gene Set

external female genital organ Gene Set

Genital Herpes Gene Set

Recurrent Genital Herpes Simplex Gene Set

Chlamydia Trachomatis Infection Of Genital Structure Gene Set

Genital Ulcers Gene Set

Branchio-Skeleto-Genital Syndrome Gene Set

Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies Gene Set

Genital Lichen Planus Gene Set

Genital Lichen Sclerosus Gene Set

Genital Infantilism Gene Set

Autosomal Recessive Facio-Digito-Genital Syndrome Gene Set