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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
autosomal dominant distal hereditary motor neuronopathy 1  
Charcot Marie Tooth Type 1 Aplasia Cutis Congenita 
Charcot-Marie-Tooth disease intermediate type +   
Charcot-Marie-Tooth disease type 1 +   
Charcot-Marie-Tooth disease type 2 +   
Charcot-Marie-Tooth disease type 3  
Charcot-Marie-Tooth disease type 4 +   
A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance. (DO)
Charcot-Marie-Tooth disease type 5  
Charcot-Marie-Tooth disease type 6 +   
Charcot-Marie-Tooth disease type 7 
Charcot-Marie-Tooth disease type X +   
Charcot-Marie-Tooth Disease with Ptosis and Parkinsonism 
Charcot-Marie-Tooth Disease, Guadalajara Neuronal Type 
Charcot-Marie-Tooth Peroneal Muscular Atrophy and Friedreich Ataxia, Combined 
congenital vertical talus  
Mitochondrial Form of Axonal Charcot-Marie-Tooth Disease 1 
Mixed Polyneuropathy of Early Onset 
Palmoplantar Keratoderma, Spastic Paralysis 

Synonyms
Exact Synonyms: Charcot-Marie-Tooth disease, type IV ;   Charcot-Marie-Tooth, type 4 ;   hereditary motor and sensory neuropathy ;   hereditary motor and sensory neuropathy 4
Xrefs: GARD:12440 ;   ORDO:64749
Definition Sources: http://www.ninds.nih.gov/disorders/charcot_marie_tooth/detail_charcot_marie_tooth.htm "DO" "DO"

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