chromosome 17p13.3 duplication syndrome

Summary
Synonym
  • 17p13.3 duplication syndrome
  • 17p13.3 microduplication syndrome
  • chromosome 17p13.3 centromeric duplication syndrome
  • trisomy 17p13.3
Definition
A chromosomal duplication syndrome that has_material_basis_in duplication of the chromosome 17p13.3 region.
Super Class
chromosomal duplication syndrome
External Links
Disease Ontology
DOID:0060432
Mondo Disease Ontology
MeSH
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5048 PAFAH1B1 platelet activating factor acetylhydrolase 1b regulatory subunit 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P43034 Platelet-activating factor acetylhydrolase IB subunit beta
The Human Phenotype Ontology
Displaying entries 1 - 10 of 19 in total
HPO ID HPO Term
HP:0000445 Wide nose
HP:0002119 Ventriculomegaly
HP:0000218 High palate
HP:0001263 Global developmental delay
HP:0000098 Tall stature
HP:0002007 Frontal bossing
HP:0000348 High forehead
HP:0004209 Clinodactyly of the 5th finger
HP:0000494 Downslanted palpebral fissures
HP:0000023 Inguinal hernia
Displaying 1 entry
Gene ID Gene Symbol Description
5048 PAFAH1B1 platelet activating factor acetylhydrolase 1b regulatory subunit 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