infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
MONDO:0018705Mondo
Findings
No curated finding names infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
26 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.
- Abnormal peripheral action potential amplitudeHPOHP:0030179
- Frequent (30% to 79% of cases)
- Absent speechHPOHP:0001344
- Frequent (30% to 79% of cases)
- Bilateral tonic-clonic seizureHPOHP:0002069
- Frequent (30% to 79% of cases)
- Cerebral atrophyHPOHP:0002059
- Frequent (30% to 79% of cases)
- CryptorchidismHPOHP:0000028
- Frequent (30% to 79% of cases)
- Decreased nerve conduction velocityHPOHP:0000762
- Frequent (30% to 79% of cases)
- DyskinesiaHPOHP:0100660
- Frequent (30% to 79% of cases)
- DystoniaHPOHP:0001332
- Frequent (30% to 79% of cases)
- EEG abnormalityHPOHP:0002353
- Frequent (30% to 79% of cases)
- Feeding difficulties in infancyHPOHP:0008872
- Frequent (30% to 79% of cases)
- Floppy infantHPOHP:0008947
- Frequent (30% to 79% of cases)
- Foot joint contractureHPOHP:0008366
- Frequent (30% to 79% of cases)
Show the remaining 14
- Functional motor deficitHPOHP:0004302
- Frequent (30% to 79% of cases)
- Gastroesophageal refluxHPOHP:0002020
- Frequent (30% to 79% of cases)
- Gastrostomy tube feeding in infancyHPOHP:0011471
- Frequent (30% to 79% of cases)
- GlaucomaHPOHP:0000501
- Frequent (30% to 79% of cases)
- Global developmental delayHPOHP:0001263
- Frequent (30% to 79% of cases)
- Horizontal supranuclear gaze palsyHPOHP:0007817
- Frequent (30% to 79% of cases)
Where it sits
- A kind of
Other names
2 names
Resolves to: infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome
- Also called
- ANOACaxonal neuropathy-optic atrophy-cognitive deficit syndrome