microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum
MONDO:0032656Mondo
Findings
No curated finding names microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
15 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.
- Attention deficit hyperactivity disorderHPOHP:0007018
- 4 of 4 reported patients
- Babinski signHPOHP:0003487
- 4 of 4 reported patients
- Cogwheel rigidityHPOHP:0002396
- 4 of 4 reported patients
- Decreased body weightHPOHP:0004325
- 4 of 4 reported patients
- Delayed gross motor developmentHPOHP:0002194
- 4 of 4 reported patients
- Developmental cataractHPOHP:0000519
- 4 of 4 reported patients · Congenital onset
- DysarthriaHPOHP:0001260
- 4 of 4 reported patients
- DystoniaHPOHP:0001332
- 4 of 4 reported patients
- Growth delayHPOHP:0001510
- 4 of 4 reported patients
- Intellectual disabilityHPOHP:0001249
- 4 of 4 reported patients
- MicrocephalyHPOHP:0000252
- 4 of 4 reported patients
- Short statureHPOHP:0004322
- 4 of 4 reported patients
Show the remaining 3
- Spastic gaitHPOHP:0002064
- 4 of 4 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 3 of 4 reported patients
- GlaucomaHPOHP:0000501
- 1 of 4 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- KCNA4HGNC:6222
- Limited · Ambry Genetics · Autosomal recessive · 2018
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2020
- Limited · G2P · Autosomal recessive · 2025
Where it sits
- A kind of