Disease #01841 (CNSHA5 (anemia, congenital, nonspherocytic hemolytic, type 5, hexokinase deficient), OMIM:235700)

Official abbreviation	CNSHA5
Name	anemia, congenital, nonspherocytic hemolytic, type 5, hexokinase deficient
OMIM ID	235700
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HK1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2026-06-26 18:53:58 +02:00 (CEST)

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