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DO Term : Charcot-Marie-Tooth disease type 2 [DOID:0050539] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.

synonyms:
604484,
ICD9CM:356.0,
SNOMEDCT_US_2023_03_01:193158000,
OMIM:604484,
OMIM:118230,
GARD:12431,
ORDO:64746,
UMLS_CUI:C0392553,
hereditary motor and sensory neuropathy type 2,
hereditary motor and sensory neuropathy Guadalajara neuronal type,
118230,
hereditary motor and sensory neuropathy Okinawa type

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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