Neuronopathy, distal hereditary motor, type 2D

Definition

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the FBXO38 gene.

Also known as FBXO38 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in FBXO38 — per MONDO

Also identified as

• DOID 0111210 per MONDO
• OMIM 615575 per MONDO
• UMLS C3888271 per MONDO