Disease #00538 (hypoproteinemia (hypoproteinemia, hypercatabolic, familial (FHH)), OMIM:241600)

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	Curator: Johan T. den Dunnen

Official abbreviation	hypoproteinemia
Name	hypoproteinemia, hypercatabolic, familial (FHH)
OMIM ID	241600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	B2M
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-24 22:35:18 +02:00 (CEST)
Date last edited	N/A