Baralle-Macken syndrome
MONDO:0031002Mondo
Findings
No curated finding names Baralle-Macken syndrome 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
24 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
- 6 of 6 reported patients
- Delayed ability to walkHPOHP:0031936
- 6 of 6 reported patients
- High, narrow palateHPOHP:0002705
- 2 of 2 reported patients
- Neonatal hypotoniaHPOHP:0001319
- 2 of 2 reported patients
- Severe intellectual disabilityHPOHP:0010864
- 6 of 6 reported patients
- Tapered fingerHPOHP:0001182
- 2 of 2 reported patients
- Upslanted palpebral fissureHPOHP:0000582
- 2 of 2 reported patients
- Delayed speech and language developmentHPOHP:0000750
- 5 of 6 reported patients
- MicrocephalyHPOHP:0000252
- 5 of 6 reported patients
- Inability to walkHPOHP:0002540
- 4 of 6 reported patients
- SpasticityHPOHP:0001257
- 4 of 6 reported patients
- Absent speechHPOHP:0001344
- 2 of 6 reported patients
Show the remaining 12
- Acanthosis nigricansHPOHP:0000956
- 2 of 6 reported patients
- HirsutismHPOHP:0001007
- 2 of 6 reported patients
- KyphosisHPOHP:0002808
- 2 of 6 reported patients
- ObesityHPOHP:0001513
- 2 of 6 reported patients
- Striae distensaeHPOHP:0001065
- 2 of 6 reported patients
- Urinary incontinenceHPOHP:0000020
- 2 of 6 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.
- COPB1HGNC:2231
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
- Limited · G2P · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
2 names
Resolves to: Baralle-Macken syndrome
- Also called
- BARMACSneurodevelopmental disorder with cataracts and variable microcephaly