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temtamy preaxial brachydactyly syndrome
Summary
- Synonym
-
- PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
- Definition
- A syndrome that is characterized by brachydactyly, hyperphalangism of digits, facial dysmorphism, dental anomalies, sensorineural hearing loss, delayed motor and mental development, and growth retardation and has_material_basis_in homozygous mutation in the CHSY1 gene.
- Super Class
- autosomal recessive disease syndrome
External Links
- Disease Ontology
- DOID:0050814
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 100036707 | chsy1 | chondroitin sulfate synthase 1 | Xenopus tropicalis (tropical clawed frog) | |
| 108711484 | chsy1.L | chondroitin sulfate synthase 1 L homeolog | Xenopus laevis (African clawed frog) | |
| 108712816 | chsy1.S | chondroitin sulfate synthase 1 S homeolog | Xenopus laevis (African clawed frog) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q86X52 | Chondroitin sulfate synthase 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000160 | Narrow mouth |
| HP:0000164 | Abnormality of the dentition |
| HP:0000311 | Round face |
| HP:0000327 | Hypoplasia of the maxilla |
| HP:0000347 | Micrognathia |
| HP:0000369 | Low-set ears |
| HP:0000517 | Abnormal lens morphology |
| HP:0000592 | Blue sclerae |
| HP:0000648 | Optic atrophy |
| HP:0000668 | Hypodontia |
