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Metadata
ID DOID:10923
Name sickle cell anemia
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.
https://en.wikipedia.org/wiki/Sickle_cell_disease, https://ghr.nlm.nih.gov/condition/sickle-cell-disease, https://www.nhlbi.nih.gov/health-topics/sickle-cell-disease
Xrefs

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_2022_03_01:154798006

SNOMEDCT_US_2022_03_01:35434009

UMLS_CUI:C0002895

UMLS_CUI:C0019034

Alternateids

DOID:12924

DOID:13024

Subsets

NCIthesaurus

Synonyms

drepanocytosis [EXACT]

haemoglobin SC disease [EXACT]

Hb SC disease [EXACT]

Hb-S/Hb-C disease [EXACT]

Hb-SS disease without crisis [EXACT]

Hemoglobin S disease without crisis [EXACT]

hemoglobin SC disease [EXACT]

sickle cell anaemia [EXACT]

Sickle-cell/Hb-C disease without crisis [EXACT]

Parent Relationships

is_a blood protein disease

is_a autosomal recessive disease

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