Disease #00017 (THPH3 (THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT), OMIM:176860)

Labor Staber Humangenetik

LOVD v.3.0 Build 29 [ Current LOVD status ]
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	Curators: Sabine Heber and Florian Bayersdorfer

Official abbreviation	THPH3
Name	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL DOMINANT
OMIM ID	176860
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PROC
Associated tissues	-
Disease features	-
Remarks	-