Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	GRISCELLI SYNDROME, TYPE 3
Synonyms	GS3
ID	http://purl.bioontology.org/ontology/OMIM/609227
altLabel	GS3
cui	C1836573
Gene Locus	2q37
Gene Symbol	MLPH
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU001093 http://purl.bioontology.org/ontology/OMIM/MTHU042944 http://purl.bioontology.org/ontology/OMIM/MTHU001092 http://purl.bioontology.org/ontology/OMIM/MTHU001090 http://purl.bioontology.org/ontology/OMIM/MTHU029857 http://purl.bioontology.org/ontology/OMIM/MTHU001096 http://purl.bioontology.org/ontology/OMIM/MTHU001091 http://purl.bioontology.org/ontology/OMIM/MTHU029858 http://purl.bioontology.org/ontology/OMIM/MTHU029859 http://purl.bioontology.org/ontology/OMIM/MTHU001089
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	609227
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	GRISCELLI SYNDROME, TYPE 3
tui	T047

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0060834	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/MESH/C537303	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/C537303	Medical Subject Headings	LOOM