ZFIN Human Disease: hereditary spherocytosis

OBO ID: DOID:12971

Term Name:	hereditary spherocytosis		Search Ontology:
Synonyms:	Congenital spherocytic hemolytic anemia Minkowski Chauffard syndrome spherocytic anemia
Definition:	A congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape. (2)
References:	GARD:6639 ICD10CM:D58.0 ICD9CM:282.0 MESH:D013103 NCI:C97074 ORDO:822 SNOMEDCT_US_2023_03_01:154795009 UMLS_CUI:C0037889
Ontology:	Human Disease ( DOID:12971 )

Relationships

is a type of:	congenital hemolytic anemia congenital hemolytic anemia Show first 5 Terms
has subtype:	hereditary spherocytosis type 1 hereditary spherocytosis type 2 hereditary spherocytosis type 3 hereditary spherocytosis type 4 hereditary spherocytosis type 5 hereditary spherocytosis type 1 hereditary spherocytosis type 2 hereditary spherocytosis type 3 hereditary spherocytosis type 4 hereditary spherocytosis type 5 Show first 5 Terms

OTHER hereditary spherocytosis PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None