Disease #01780 (F10D (deficiency, factor X (F10D)), OMIM:227600)

Official abbreviation F10D
Name deficiency, factor X (F10D)
OMIM ID 227600
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene F10
Associated tissues -
Disease features -
Remarks -