neuronopathy, distal hereditary motor, type 5
MONDO:0100350Mondo
Findings
No curated finding names neuronopathy, distal hereditary motor, type 5 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
16 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Cold-induced hand crampsHPOHP:0003435
- Frequent (30% to 79% of cases)
- Distal amyotrophyHPOHP:0003693
- Frequent (30% to 79% of cases)
- Distal lower limb muscle weaknessHPOHP:0009053
- Frequent (30% to 79% of cases)
- First dorsal interossei muscle atrophyHPOHP:0003426
- Frequent (30% to 79% of cases)
- First dorsal interossei muscle weaknessHPOHP:0003392
- Frequent (30% to 79% of cases)
- Impaired vibratory sensationHPOHP:0002495
- Frequent (30% to 79% of cases)
- Motor polyneuropathyHPOHP:0007178
- Frequent (30% to 79% of cases)
- Thenar muscle atrophyHPOHP:0003393
- Frequent (30% to 79% of cases)
- Thenar muscle weaknessHPOHP:0003427
- Frequent (30% to 79% of cases)
- Unsteady gaitHPOHP:0002317
- Frequent (30% to 79% of cases)
- Upper limb muscle weaknessHPOHP:0003484
- Frequent (30% to 79% of cases)
- HammertoeHPOHP:0001765
- Occasional (5% to 29% of cases)
Show the remaining 4
- HyperreflexiaHPOHP:0001347
- Occasional (5% to 29% of cases)
- Pes cavusHPOHP:0001761
- Occasional (5% to 29% of cases)
- Pes valgusHPOHP:0008081
- Occasional (5% to 29% of cases)
- Abnormal motor nerve conduction velocityHPOHP:0040131
- Very rare (1% to 4% of cases)
Where it sits
Other names
3 names
Resolves to: neuronopathy, distal hereditary motor, type 5
- Also called
- distal hereditary motor neuropathy type Vdistal HMN Vdistal spinal muscular atrophy type 5