Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Catel Manzke syndrome
Summary
- Synonym
-
- Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome
- Micrognathia digital syndrome
- Definition
- A bone disease that is characterized by the Pierre Robin anomaly, which comprises cleft palate, glossoptosis, and micrognathia, and a unique form of bilateral hyperphalangy in which there is an accessory bone inserted between the second metacarpal and its corresponding proximal phalanx, resulting in radial deviation of the index finger and that has_material_basis_in homozygous or compound heterozygous mutation in the TGDS gene on chromosome 13q32.
- Super Class
- bone disease
External Links
- Disease Ontology
- DOID:0081122
- Mondo Disease Ontology
- MeSH
- ORDO
- OMIM
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002553 | Highly arched eyebrow |
| HP:0000389 | Chronic otitis media |
| HP:0030680 | Abnormal cardiovascular system morphology |
| HP:0000293 | Full cheeks |
| HP:0005930 | Abnormal epiphysis morphology |
| HP:0001508 | Failure to thrive |
| HP:0000175 | Cleft palate |
| HP:0004209 | Clinodactyly of the 5th finger |
| HP:0001382 | Joint hypermobility |
| HP:0010285 | Oral synechia |
