GOLM1, golgi membrane protein 1, 51280

N. diseases: 100; N. variants: 3
Disease: Hereditary spherocytosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		0.010 GeneticVariation disease BEFREE Next‑generation sequencing was used, and the genetic source of HS was identified as a GOLM1 gene mutation. 30896804 2019