Disease #03110 (SHEP-10 (pigmentation, skin/hair/eye, variation in, type 10 (SHEP-10)), OMIM:612267)

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 -
Phenotype entries for this disease -
Associated with 1 gene TPCN2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A

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