neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
MONDO:0060664Mondo
Findings
No curated finding names neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities 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
- Infantile onset
HPO, annotations 2026-09-02
Features
33 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.
- CataractHPOHP:0000518
- 3 of 3 reported patients
- Gastroesophageal refluxHPOHP:0002020
- 3 of 3 reported patients
- MicrocephalyHPOHP:0000252
- 3 of 3 reported patients
- SeizureHPOHP:0001250
- 3 of 3 reported patients
- Severe global developmental delayHPOHP:0011344
- 3 of 3 reported patients
- HypotoniaHPOHP:0001252
- 2 of 3 reported patients
- Absent speechHPOHP:0001344
- 1 of 3 reported patients
- AminoaciduriaHPOHP:0003355
- 1 of 3 reported patients
- Brain atrophyHPOHP:0012444
- 1 of 3 reported patients
- Congenital hip dislocationHPOHP:0001374
- 1 of 3 reported patients
- Delayed CNS myelinationHPOHP:0002188
- 1 of 3 reported patients
- Epiphyseal dysplasiaHPOHP:0002656
- 1 of 3 reported patients
Show the remaining 21
- Feeding difficultiesHPOHP:0011968
- 1 of 3 reported patients
- Growth delayHPOHP:0001510
- 1 of 3 reported patients
- High palateHPOHP:0000218
- 1 of 3 reported patients
- HydronephrosisHPOHP:0000126
- 1 of 3 reported patients
- HypertensionHPOHP:0000822
- 1 of 3 reported patients
- HypocalcemiaHPOHP:0002901
- 1 of 3 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.
- GEMIN4HGNC:15717
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · G2P · Autosomal recessive · 2020
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2022