ZFIN Human Disease: Griscelli syndrome

OBO ID: DOID:0060831

Term Name:	Griscelli syndrome		Search Ontology:
Synonyms:	Chediak-Higashi-like syndrome Griscelli-Prunieras syndrome partial albinism-immunodeficiency syndrome
Definition:	An integumentary system disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin. (2)
References:	GARD:10913 ICD10CM:E70.3 OMIM:PS214450 ORDO:381
Ontology:	Human Disease ( DOID:0060831 )

Relationships

is a type of:	autosomal recessive disease integumentary system disease autosomal recessive disease integumentary system disease Show first 5 Terms
has subtype:	Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS (1)