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

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 -
Date created 2016-07-08 14:33:15 +00:00 (UTC)
Date last edited 2023-06-16 09:55:17 +00:00 (UTC)