ZFIN Human Disease: congenital nonspherocytic hemolytic anemia

OBO ID: DOID:2861

Term Name:	congenital nonspherocytic hemolytic anemia		Search Ontology:
Synonyms:	congenital nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anaemia hereditary nonspherocytic hemolytic anemia HNSHA
Definition:
References:	MESH:D000746 OMIM:206300 OMIM:206400 OMIM:300908 OMIM:613470 ORDO:712 SNOMEDCT_US_2023_03_01:82775009 UMLS_CUI:C0002882
Ontology:	Human Disease ( DOID:2861 )

Relationships

is a type of:	congenital hemolytic anemia congenital hemolytic anemia Show first 5 Terms
has subtype:	Heinz body anemia pyruvate kinase deficiency of red cells Heinz body anemia pyruvate kinase deficiency of red cells Show first 5 Terms

OTHER congenital nonspherocytic hemolytic anemia PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
G6PD	g6pd	Hemolytic anemia, G6PD deficient (favism)	300908
GPI	gpib gpia	Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency	613470

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None