Disease #00455 (HMN-1 (neuropathy, motor, distal, hereditary, type I (HMN-1)), OMIM:182960)

Official abbreviation HMN-1
Name neuropathy, motor, distal, hereditary, type I (HMN-1)
OMIM ID 182960
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
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00017871 - PubMed: Puls 2003 4-generation family, 12 affecteds (8F, 4M) - no United States - - 0 - - HMN-1 see paper; motor neuron disease, lower DCTN1 DCTN1 1 12 Johan den Dunnen
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