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MIRAGE
holoprosencephaly 9
Summary
- Synonym
-
- HPE9
- holoprosencephaly with microphthalmia and first branchial arch anomalies
- pituitary anomalies with holoprosencephaly-like features
- Definition
- A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.
- Super Class
- autosomal dominant disease holoprosencephaly
External Links
- Disease Ontology
- DOID:0110873
- MeSH
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P10070 | Zinc finger protein GLI2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000119 | Abnormality of the genitourinary system |
| HP:0000161 | Median cleft upper lip |
| HP:0000175 | Cleft palate |
| HP:0000193 | Bifid uvula |
| HP:0000218 | High palate |
| HP:0000238 | Hydrocephalus |
| HP:0000252 | Microcephaly |
| HP:0000256 | Macrocephaly |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000457 | Depressed nasal ridge |
