ZFIN Human Disease: hereditary spherocytosis type 3

OBO ID: DOID:0110918

OBO ID: DOID:0110918

Term Name:	hereditary spherocytosis type 3	Search Ontology:
Synonyms:	hereditary spherocytosis 3 HS3 SPH3
Definition:	A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1. https://www.ncbi.nlm.nih.gov/pubmed/8941647
References:	OMIM:270970
Ontology:	Human Disease ( DOID:0110918 )

Relationships

is a type of:	autosomal recessive disease hereditary spherocytosis autosomal recessive disease hereditary spherocytosis Show first 5 Terms

OTHER hereditary spherocytosis type 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SPTA1		Spherocytosis, type 3

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None