craniometaphyseal dysplasia, autosomal recessive
Findings
No curated finding names craniometaphyseal dysplasia, autosomal recessive yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Autosomal recessive form of craniometaphyseal dysplasia.
Definition from the Mondo Disease Ontology (MONDO:0009035), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
4 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.
- Depressed nasal ridgeHPOHP:0000457
- 5 of 5 reported patients
- Facial hyperostosisHPOHP:0005465
- 5 of 5 reported patients
- HypertelorismHPOHP:0000316
- 5 of 5 reported patients
- Intellectual disabilityHPOHP:0001249
- 0 of 5 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.
- GJA1HGNC:4274
- Limited · Ambry Genetics · Autosomal recessive · 2020
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2019
Where it sits
Other names
1 name
Resolves to: craniometaphyseal dysplasia, autosomal recessive
- Also called
- autosomal recessive craniometaphyseal dysplasia