Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	DYSFIBRINOGENEMIA, CONGENITAL
Synonyms	HYPODYSFIBRINOGENEMIA, CONGENITAL
ID	http://purl.bioontology.org/ontology/OMIM/616004
altLabel	HYPODYSFIBRINOGENEMIA, CONGENITAL
cui	C1859970 C0272350
Gene Locus	4q28
Gene Symbol	FGG
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	616004
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	DYSFIBRINOGENEMIA, CONGENITAL
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/C565970	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10CM/D68.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/C562727	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C562727	Medical Subject Headings	LOOM