Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I
Synonyms	CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2I
ID	http://purl.bioontology.org/ontology/OMIM/607677
altLabel	CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2I CMT2I
cui	C3888087
Gene Locus	1q22
Gene Symbol	CMTDID CHM MPZ CMT1B DSS
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU002722 http://purl.bioontology.org/ontology/OMIM/MTHU000902 http://purl.bioontology.org/ontology/OMIM/MTHU000328 http://purl.bioontology.org/ontology/OMIM/MTHU000326 http://purl.bioontology.org/ontology/OMIM/MTHU002901 http://purl.bioontology.org/ontology/OMIM/MTHU029675 http://purl.bioontology.org/ontology/OMIM/MTHU000909 http://purl.bioontology.org/ontology/OMIM/MTHU029674 http://purl.bioontology.org/ontology/OMIM/MTHU000325 http://purl.bioontology.org/ontology/OMIM/MTHU002899 http://purl.bioontology.org/ontology/OMIM/MTHU001014 http://purl.bioontology.org/ontology/OMIM/MTHU001004 http://purl.bioontology.org/ontology/OMIM/MTHU000335 http://purl.bioontology.org/ontology/OMIM/MTHU000329 http://purl.bioontology.org/ontology/OMIM/MTHU000900
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	607677
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I
tui	T047

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/C535416	Medical Subject Headings	CUI