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Yunis-Varon syndrome
Summary
- Synonym
-
- cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia
- cleidocranial dysplasia-micrognathia-absent thumbs syndrome
- Definition
- A syndrome characterized by skeletal defects, including cleidocranial dysplasia and digital anomalies, and severe neurologic involvement with neuronal loss. Enlarged cytoplasmic vacuoles are found in neurons, muscle, and cartilage. It is usually lethal in infancy and has_material_basis_in homozygous or compound heterozygous mutation in the FIG4 gene on chromosome 6q21.
- Super Class
- autosomal recessive disease syndrome
External Links
- Disease Ontology
- DOID:0060589
- Mondo Disease Ontology
- MeSH
- UMLS
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0010537 | Wide cranial sutures |
| HP:0010880 | Increased nuchal translucency |
| HP:0011061 | Abnormality of dental structure |
| HP:0011451 | Primary microcephaly |
| HP:0012294 | Abnormal occipital bone morphology |
| HP:0012809 | Narrow nasal base |
| HP:0100817 | Renovascular hypertension |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000187 | Broad alveolar ridges |
| HP:0000218 | High palate |
