Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024

Preferred Name	DYSFIBRINOGENEMIA, CONGENITAL
Synonyms	HYPODYSFIBRINOGENEMIA, CONGENITAL
ID	http://purl.bioontology.org/ontology/OMIM/616004
altLabel	HYPODYSFIBRINOGENEMIA, CONGENITAL
cui	C0272350 C1859970
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
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRGER/10051123	MDRGER	CUI
http://purl.bioontology.org/ontology/MESH/C565970	MESH	CUI
http://purl.bioontology.org/ontology/MDRGER/10054362	MDRGER	CUI
http://purl.bioontology.org/ontology/MEDDRA/10051123	MEDDRA	CUI
http://purl.bioontology.org/ontology/ICD10CM/D68.2	ICD10CM	CUI
http://purl.bioontology.org/ontology/SNMI/DC-64010	SNMI	CUI
http://purl.bioontology.org/ontology/MDRFRE/10054362	MDRFRE	CUI
http://purl.bioontology.org/ontology/MDRFRE/10051123	MDRFRE	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/45366001	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MEDDRA/10054362	MEDDRA	CUI
http://purl.bioontology.org/ontology/MESH/C562727	MESH	CUI
http://purl.bioontology.org/ontology/SCTSPA/45366001	SCTSPA	CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C562727	RH-MESH	LOOM
http://purl.bioontology.org/ontology/MESH/C562727	MESH	LOOM