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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
holoprosencephaly
Summary
- Synonym
-
- Holoprosencephaly sequence
- Definition
- A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies.
- Super Class
- congenital nervous system abnormality syndrome
External Links
- Disease Ontology
- DOID:4621
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 171881 | pign-1 | GPI ethanolamine phosphate transferase 1 | |
| 173631 | ptc-3 | Protein patched homolog 3 | |
| 174274 | ptc-1 | Protein patched homolog 1;SSD domain-containing protein | |
| 179556 | pgap-1 | GPI inositol-deacylase | |
| 180349 | grd-2 | Ground-like domain-containing protein | |
| 180638 | wrt-6 | Warthog protein 6 N-product |
