familial digital arthropathy-brachydactyly

Summary

familial digital arthropathy-brachydactyly is a developmental defect during embryogenesis^[1].

Key Facts

• familial digital arthropathy-brachydactyly's instance of is recorded as developmental defect during embryogenesis^[2].
• familial digital arthropathy-brachydactyly's instance of is recorded as rare disease^[3].
• familial digital arthropathy-brachydactyly's instance of is recorded as class of disease^[4].
• familial digital arthropathy-brachydactyly's subclass of is recorded as syndrome with brachydactyly^[5].
• familial digital arthropathy-brachydactyly's subclass of is recorded as TRPV4-related bone disorder^[6].
• familial digital arthropathy-brachydactyly's MeSH descriptor ID is recorded as C564656^[7].
• familial digital arthropathy-brachydactyly's OMIM ID is recorded as 606835^[8].
• familial digital arthropathy-brachydactyly's KEGG ID is recorded as H02062^[9].
• familial digital arthropathy-brachydactyly's Orphanet ID is recorded as 85169^[10].
• familial digital arthropathy-brachydactyly's NCI Thesaurus ID is recorded as C175208^[11].
• familial digital arthropathy-brachydactyly's genetic association is recorded as TRPV4^[12].
• familial digital arthropathy-brachydactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85169^[13].
• familial digital arthropathy-brachydactyly's UMLS CUI is recorded as C1847406^[14].
• familial digital arthropathy-brachydactyly's ICD-10-CM is recorded as M06.8^[15].
• familial digital arthropathy-brachydactyly's Mondo ID is recorded as MONDO_0011732^[16].
• familial digital arthropathy-brachydactyly's UniProt disease ID is recorded as DI-03486^[17].