wrinkly skin syndrome

Summary
Synonym
  • WSS
Definition
A syndrome characterized by sagging or wrinkly skin, reduced skin elasticity, delayed closure of the fontanel, typically mild developmental delay, and variable other skeletal, neurological and facial features that has_material_basis_in homozygous or compound heterozygous mutation in the ATP6V0A2 gene on chromosome 12q24.31.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:0112171
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23545 ATP6V0A2 ATPase H+ transporting V0 subunit a2
The Human Phenotype Ontology
Displaying entries 21 - 30 of 85 in total
HPO ID HPO Term
HP:0001350 Slurred speech
HP:0001374 Congenital hip dislocation
HP:0001476 Delayed closure of the anterior fontanelle
HP:0001508 Failure to thrive
HP:0001511 Intrauterine growth retardation
HP:0001537 Umbilical hernia
HP:0001611 Hypernasal speech
HP:0001763 Pes planus
HP:0001788 Premature rupture of membranes
HP:0001869 Deep plantar creases
Displaying 1 entry
Gene ID Gene Symbol Description
23545 ATP6V0A2 ATPase H+ transporting V0 subunit a2

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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