ZFIN Human Disease: sickle cell anemia

OBO ID: DOID:10923

Term Name:	sickle cell anemia		Search Ontology:
Synonyms:	drepanocytosis haemoglobin SC disease Hb SC disease Hb-S/Hb-C disease Hb-SS disease without crisis Hemoglobin S disease without crisis hemoglobin SC disease sickle cell anaemia Sickle-cell/Hb-C disease without crisis
Definition:	A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape. (3)
References:	GARD:8614 ICD10CM:D57.1 ICD10CM:D57.2 ICD9CM:282.6 ICD9CM:282.63 MESH:D000755 MESH:D006450 NCI:C34383 NCI:C34676 OMIM:603903 ORDO:232 SNOMEDCT_US_2023_03_01:154798006 SNOMEDCT_US_2023_03_01:35434009 UMLS_CUI:C0002895 UMLS_CUI:C0019034
Ontology:	Human Disease ( DOID:10923 )

Relationships

is a type of:	autosomal recessive disease blood protein disease autosomal recessive disease blood protein disease Show first 5 Terms

OTHER sickle cell anemia PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HBB		Sickle cell disease

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None