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Ontology Browser

Term:
distal hereditary motor neuronopathy type 2A (DOID:0111208)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Charcot-Marie-Tooth disease axonal type 2C  
Charcot-Marie-Tooth disease axonal type 2CC  
Charcot-Marie-Tooth disease axonal type 2F  
Charcot-Marie-Tooth disease axonal type 2H 
Charcot-Marie-Tooth disease axonal type 2K  
Charcot-Marie-Tooth disease axonal type 2L  
Charcot-Marie-Tooth disease axonal type 2N  
Charcot-Marie-Tooth disease axonal type 2O  
Charcot-Marie-Tooth disease axonal type 2P  
Charcot-Marie-Tooth disease axonal type 2Q  
Charcot-Marie-Tooth disease axonal type 2S  
Charcot-Marie-Tooth disease axonal type 2T  
Charcot-Marie-Tooth disease axonal type 2U  
Charcot-Marie-Tooth disease axonal type 2V  
Charcot-Marie-Tooth disease axonal type 2X  
Charcot-Marie-Tooth disease axonal type 2Z  
Charcot-Marie-Tooth disease type 2B  
Charcot-Marie-Tooth disease type 2B1  
Charcot-Marie-Tooth disease type 2B2  
Charcot-Marie-Tooth disease type 2D  
Charcot-Marie-Tooth disease type 2DD  
Charcot-Marie-Tooth disease type 2E  
Charcot-Marie-Tooth disease type 2EE  
Charcot-Marie-Tooth disease type 2I  
Charcot-Marie-Tooth disease type 2J  
Charcot-Marie-Tooth disease type 2R  
Charcot-Marie-Tooth disease type 2Y  
Charcot-Marie-Tooth disease, axonal type 2W  
Charcot-Marie-Tooth Disease, Type 2A +   
distal hereditary motor neuronopathy type 2A  
A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in HSPB8 on 12q24.23. (DO)
distal hereditary motor neuronopathy type 2C  
distal hereditary motor neuronopathy type 2D  
distal hereditary motor neuropathy type 2B  
Hereditary Motor and Sensory Neuropathy, Okinawa Type  

Synonyms
Exact Synonyms: Charcot-Marie-Tooth Disease, Spinal, IIA ;   DHMN2A ;   HMN IIA ;   HMN2A ;   autosomal dominant adult spinal muscular atrophy IIA ;   distal hereditary motor neuronopathy, type IIA ;   distal hereditary motor neuropathy type IIA ;   distal spinal muscular atrophy, adult autosomal dominant, IIA
Primary IDs: MESH:C563561
Alternate IDs: OMIM:158590 ;   RDO:0012786
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/15122253 "DO"

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