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Ontology Browser
Term:
autosomal dominant distal hereditary motor neuronopathy 2 (DOID:0111206)
Annotations: Rat: (4) Mouse: (4) Human: (4) Chinchilla: (4) Bonobo: (4) Dog: (4) Squirrel: (4) Pig: (4) Naked Mole-rat: (4) Green Monkey: (4)
Parent Terms Term With Siblings Child Terms
autosomal dominant distal hereditary motor neuronopathy 1  
autosomal dominant distal hereditary motor neuronopathy 10  
autosomal dominant distal hereditary motor neuronopathy 11  
autosomal dominant distal hereditary motor neuronopathy 12  
autosomal dominant distal hereditary motor neuronopathy 13  
autosomal dominant distal hereditary motor neuronopathy 14  
autosomal dominant distal hereditary motor neuronopathy 15  
autosomal dominant distal hereditary motor neuronopathy 2  
An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy with onset between 15 to 25 years of age and that has_material_basis_in heterozygous mutation in the gene encoding heat-shock 22-kD protein-8 (HSPB8) on chromosome 12q24. (DO)
autosomal dominant distal hereditary motor neuronopathy 3  
autosomal dominant distal hereditary motor neuronopathy 4  
autosomal dominant distal hereditary motor neuronopathy 5  
autosomal dominant distal hereditary motor neuronopathy 6  
autosomal dominant distal hereditary motor neuronopathy 7  
autosomal dominant distal hereditary motor neuronopathy 8  
autosomal dominant distal hereditary motor neuronopathy 9  
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 2FF  
Charcot-Marie-Tooth disease axonal type 2H 
Charcot-Marie-Tooth Disease Axonal Type 2HH  
Charcot-Marie-Tooth Disease Axonal Type 2II  
Charcot-Marie-Tooth disease axonal type 2JJ  
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 +   
Hereditary Motor and Sensory Neuropathy, Okinawa Type  

Synonyms
Exact Synonyms: Charcot-Marie-Tooth disease, spinal, IIA ;   DHMN2A ;   HMN II ;   HMN IIA ;   HMN2 ;   HMN2A ;   HMND2 ;   autosomal dominant adult spinal muscular atrophy IIA ;   distal hereditary motor neuronopathy type 2 ;   distal hereditary motor neuronopathy type 2A
Alternate IDs: DOID:0111208
Xrefs: MESH:C563561 ;   MIM:158590 ;   MONDO:0008025 ;   ORDO:139525
Definition Sources: PMID:15122253 "DO" "DO", PMID:1517763 "DO" "DO", PMID:15358725 "DO" "DO"

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