Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	MEACHAM SYNDROME
ID	http://purl.bioontology.org/ontology/OMIM/608978
cui	C1837026
Gene Locus	11p13
Gene Symbol	NPHS4 WT1
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	608978
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	MEACHAM SYNDROME
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/C538162	Medical Subject Headings	CUI