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 61 - 70 of 85 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000252 Microcephaly
HP:0000260 Wide anterior fontanel
HP:0000270 Delayed cranial suture closure
HP:0000308 Microretrognathia
HP:0000431 Wide nasal bridge
HP:0000592 Blue sclerae
HP:0000691 Microdontia
HP:0001249 Intellectual disability
HP:0001252 Hypotonia
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

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Last updated: August 19, 2024