Disease #03110

Official abbreviation SHEP-10
Name pigmentation, skin/hair/eye, variation in, type 10 (SHEP-10)
OMIM ID 612267
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TPCN2
Associated tissues -
Disease features -
Remarks -