striatonigral degeneration, infantile, mitochondrial
MONDO:0010774Mondo
Findings
No curated finding names striatonigral degeneration, infantile, mitochondrial yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Mitochondrial inheritance
- Onset and course
- Infantile onset · Childhood onset
HPO, annotations 2026-09-02
Features
19 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.
- Brisk reflexesHPOHP:0001348
- 2 of 2 reported patients
- Frequent fallsHPOHP:0002359
- 1 of 1 reported patient
- Gait disturbanceHPOHP:0001288
- 1 of 1 reported patient · Childhood onset
- Intellectual disabilityHPOHP:0001249
- 2 of 2 reported patients
- Babinski signHPOHP:0003487
- 2 of 3 reported patients
- Global developmental delayHPOHP:0001263
- 2 of 3 reported patients
- ChoreaHPOHP:0002072
- 1 of 2 reported patients
- ClonusHPOHP:0002169
- 1 of 2 reported patients
- Facial grimacingHPOHP:0000273
- 1 of 2 reported patients
- HeadacheHPOHP:0002315
- 1 of 2 reported patients
- IncoordinationHPOHP:0002311
- 2 of 4 reported patients
- Increased circulating lactate concentrationHPOHP:0002151
- 1 of 2 reported patients
Show the remaining 7
- Lingual dystoniaHPOHP:0031008
- 1 of 2 reported patients
- Mild microcephalyHPOHP:0040196
- 1 of 2 reported patients
- Motor ticsHPOHP:0100034
- 1 of 2 reported patients
- MyoclonusHPOHP:0001336
- 1 of 2 reported patients
- OphthalmoparesisHPOHP:0000597
- 1 of 2 reported patients
- Striatal T2 hyperintensityHPOHP:0031206
- 1 of 2 reported patients