ZFIN Human Disease: hereditary spherocytosis type 4

OBO ID: DOID:0110919

Term Name:	hereditary spherocytosis type 4		Search Ontology:
Synonyms:	hereditary spherocytosis 4 HS4 SPH4
Definition:	A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SLC4A1 gene on chromosome 17q21.31. https://www.ncbi.nlm.nih.gov/pubmed/7530501
References:	OMIM:612653
Ontology:	Human Disease ( DOID:0110919 )

Relationships

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

OTHER hereditary spherocytosis type 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLC4A1	slc4a1a slc4a1b	Spherocytosis, type 4	612653

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None