NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII; HMN8

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Summary

Literature (0)

MIM:600175 - NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIII; HMN8

Xenbase Genes: trpv4

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010839 - autosomal dominant congenital benign spinal muscular atrophy

MONDO:0010839 - autosomal dominant congenital benign spinal muscular atrophy

Disease Ontology (DO):

DOID:0111215 - autosomal dominant distal hereditary motor neuronopathy 8

DOID:0111215 - autosomal dominant distal hereditary motor neuronopathy 8