Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
0.330 GermlineCausalMutation ORPHANET ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. 23891469

2013

Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
0.330 GermlineCausalMutation ORPHANET Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia. 23891471

2013