Disease #00482 (SHEP5 (pigmentation, hair, black/non-black - eyes, dark/light - skin, dark/fair, type 5 (SHEP-5, skin/hair/eye pigmentation)), OMIM:227240)

Global Variome shared LOVD

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Official abbreviation	SHEP5
Name	pigmentation, hair, black/non-black - eyes, dark/light - skin, dark/fair, type 5 (SHEP-5, skin/hair/eye pigmentation)
OMIM ID	227240
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC45A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-24 22:27:21 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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