Disease #03118 (THPH4 (thrombophilia, hereditary, due to protein C deficiency, autosomal recessive (THPH4)), OMIM:612304)

Official abbreviation	THPH4
Name	thrombophilia, hereditary, due to protein C deficiency, autosomal recessive (THPH4)
OMIM ID	612304
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PROC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2019-12-02 15:55:56 +01:00 (CET)

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Global Variome shared LOVD