TBC1D24, TBC1 domain family member 24, 57465

N. diseases: 218; N. variants: 39
Disease: Deafness, congenital onychodystrophy, recessive form ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		0.300 GermlineCausalMutation phenotype ORPHANET The genetic basis of DOORS syndrome: an exome-sequencing study. 24291220 2014