trichorhinophalangeal syndrome type II

Summary
Synonym
  • Langer-Giedion syndrome
  • Trichorhinophalangeal dysplasia type II
  • trichorhinophalangeal syndrome type 2
Definition
A syndrome that has_material_basis_in mutation of the EXT1 and TRPS1 gene which results_in multiple exostosis along with short stature and cone-shaped ends located_in epiphysis. The disease has_symptom sparse scalp hair, has_symptom thin upper lip, has_symptom rounded nose.
Super Class
autosomal dominant disease syndrome
External Links
Disease Ontology
DOID:4998
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2131 EXT1 exostosin glycosyltransferase 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q16394 Exostosin-1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 38 in total
HPO ID HPO Term
HP:0001252 Hypotonia
HP:0007598 Bilateral single transverse palmar creases
HP:0000368 Low-set, posteriorly rotated ears
HP:0002119 Ventriculomegaly
HP:0000174 Abnormal palate morphology
HP:0002857 Genu valgum
HP:0000431 Wide nasal bridge
HP:0011069 Supernumerary tooth
HP:0001510 Growth delay
HP:0000076 Vesicoureteral reflux
Displaying 1 entry
Gene ID Gene Symbol Description
2131 EXT1 exostosin glycosyltransferase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024