cerebellar atrophy, visual impairment, and psychomotor retardation;
MONDO:0014811Mondo
Findings
No curated finding names cerebellar atrophy, visual impairment, and psychomotor retardation; yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
29 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.
- Cerebellar atrophyHPOHP:0001272
- 6 of 6 reported patients
- Corpus callosum atrophyHPOHP:0007371
- 6 of 6 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 7 of 7 reported patients
- Axial hypotoniaHPOHP:0008936
- 6 of 7 reported patients
- Brain atrophyHPOHP:0012444
- 5 of 6 reported patients
- HyporeflexiaHPOHP:0001265
- 5 of 6 reported patients
- Deeply set eyeHPOHP:0000490
- 5 of 7 reported patients
- ScoliosisHPOHP:0002650
- 5 of 7 reported patients
- Gingival overgrowthHPOHP:0000212
- 4 of 7 reported patients
- Limb hypertoniaHPOHP:0002509
- 4 of 7 reported patients
- RetrognathiaHPOHP:0000278
- 4 of 7 reported patients
- Abnormal electroretinogramHPOHP:0000512
- 3 of 6 reported patients
Show the remaining 17
- Abnormality of visual evoked potentialsHPOHP:0000649
- 3 of 6 reported patients
- Prominent fingertip padsHPOHP:0001212
- 3 of 7 reported patients
- Secondary microcephalyHPOHP:0005484
- 3 of 7 reported patients
- Short philtrumHPOHP:0000322
- 3 of 7 reported patients
- HypertelorismHPOHP:0000316
- 1 of 7 reported patients
- Low anterior hairlineHPOHP:0000294
- 1 of 7 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.
- EMC1HGNC:28957
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · G2P · Autosomal recessive · 2019
- Moderate · Ambry Genetics · Autosomal recessive · 2020
- Limited · G2P · Autosomal dominant · 2025