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X-linked chondrodysplasia punctata 2
Summary
- Synonym
-
- Conradi-Hunermann Syndrome
- Happle syndrome
- Definition
- A chondrodysplasia puncata that has_material_basis_in mutation in the gene encoding delta(8)-delta(7) sterol isomerase emopamil-binding protein on chromosome Xp11.
- Super Class
- X-linked dominant disease chondrodysplasia punctata
External Links
- Disease Ontology
- DOID:0080352
- Mondo Disease Ontology
- OMIM
- WikiPathways (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002787 | Tracheal calcification |
| HP:0002832 | Calcific stippling |
| HP:0002937 | Hemivertebrae |
| HP:0003462 | Elevated 8-dehydrocholesterol |
| HP:0003465 | Elevated 8(9)-cholestenol |
| HP:0003577 | Congenital onset |
| HP:0004241 | Stippled calcification in carpal bones |
| HP:0007431 | Congenital ichthyosiform erythroderma |
| HP:0007479 | Congenital nonbullous ichthyosiform erythroderma |
| HP:0008070 | Sparse hair |
