All diseases

12 entries on 1 page. Showing entries 1 - 12.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01438 - dysplasia, metatrophic 156530 AD 4 - TRPV4 - -
01490 - dwarfism, parastremmatic 168400 AD - - TRPV4 - -
01566 - dysplasia, spondyloepiphyseal, Maroteaux type 184095 AD - - TRPV4 - -
06177 ANFH2 ?Avascular necrosis of femoral head, primary, 2 617383 AD - - TRPV4 - -
05559 BCYM brachyolmia (BCYM) - - 19 11 PAPSS2, TRPV4 - -
01214 BCYM3 brachyolmia, type 3 (BCYM-3) 113500 AD - - TRPV4 - autosomal dominant
02575 CMT2C;HMSN2C Charcot-Marie-Tooth disease, type 2C (CMT-2C) 606071 AD - - TRPV4 - -
02610 FDAB Digital arthropathy-brachydactyly, familial 606835 AD - - TRPV4 - -
02293 HMN8 Neuronopathy, distal hereditary motor, type VIII 600175 AD 1 1 TRPV4 - -
01567 SMDK Spondylometaphyseal dysplasia, Kozlowski type 184252 AD - - TRPV4 - -
01554 SPSMA atrophy, muscular, spinal, scapuloperoneal 181405 AD - - TRPV4 - -
03357 SSQTL1 Sodium serum level quantitative trait locus 1 613508 - - - TRPV4 - -
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