SNOMED Clinical Terms - Hereditary spherocytosis due to spectrin deficiency - Terms

Preferred Name	Hereditary spherocytosis due to spectrin deficiency
Synonyms	Hereditary spherocytosis due to spectrin deficiency (disorder) Hereditary spherocytosis due to spectrin deficiency, NOS
ID	25266006
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/25266006
CONCEPTSTATUS	0
CTV3ID	XUALR
has_associated_morphology	Spherocyte
has_clinical_course	Courses
has_definitional_manifestation	Hemolysis Erythropenia
has_episodicity	Episodicities
has_finding_site	Hematopoietic system structure
has_severity	Severities
isa	Hereditary spherocytosis Disorder of hematopoietic structure
ISPRIMITIVE	1
Semantic_Type	Disease or Syndrome
SNOMEDID	DC-15110
SYNONYM FN	Hereditary spherocytosis due to spectrin deficiency (disorder)
SYNONYM IS	Hereditary spherocytosis due to spectrin deficiency, NOS
TUI	T047
UMLS_CUI	C0272032

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