Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	FRASIER SYNDROME
ID	http://purl.bioontology.org/ontology/OMIM/136680
cui	C0950122
Gene Locus	11p13
Gene Symbol	NPHS4 WT1
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU036762 http://purl.bioontology.org/ontology/OMIM/MTHU036764 http://purl.bioontology.org/ontology/OMIM/MTHU014910 http://purl.bioontology.org/ontology/OMIM/MTHU027075 http://purl.bioontology.org/ontology/OMIM/MTHU018098 http://purl.bioontology.org/ontology/OMIM/MTHU036763 http://purl.bioontology.org/ontology/OMIM/MTHU036761 http://purl.bioontology.org/ontology/OMIM/MTHU006962 http://purl.bioontology.org/ontology/OMIM/MTHU027076
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	136680
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	FRASIER SYNDROME
tui	T047

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0050438	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MESH/D052159	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D052159	Medical Subject Headings	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C122805	National Cancer Institute Thesaurus	LOOM