craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2
MONDO:0859567Mondo
Findings
No curated finding names craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 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
10 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.
- Absent speechHPOHP:0001344
- 1 of 1 reported patient
- Bilateral cleft lipHPOHP:0100336
- 1 of 1 reported patient
- Cavum septum pellucidumHPOHP:0002389
- 1 of 1 reported patient
- Flat faceHPOHP:0012368
- 1 of 1 reported patient
- Low-set earsHPOHP:0000369
- 1 of 1 reported patient
- Pectus excavatumHPOHP:0000767
- 1 of 1 reported patient
- Severe intellectual disabilityHPOHP:0010864
- 1 of 1 reported patient
- Shield chestHPOHP:0000914
- 1 of 1 reported patient
- Short neckHPOHP:0000470
- 1 of 1 reported patient
- Thoracic scoliosisHPOHP:0002943
- 1 of 1 reported patient
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.
- RAB5IFHGNC:15870
- Limited · Ambry Genetics · Autosomal recessive · 2022