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
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
Displaying 1 entry
Gene ID Gene Symbol Description Source
21871 Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2
Displaying all 3 entries
Gene ID Gene Symbol Description Source
174743 vha-6 V-type proton ATPase 116 kDa subunit a 3
177626 vha-5 V-type proton ATPase 116 kDa subunit a 2
178219 vha-7 V-type proton ATPase 116 kDa subunit a 4
The Human Phenotype Ontology
Displaying entries 21 - 30 of 85 in total
HPO ID HPO Term
HP:0000767 Pectus excavatum
HP:0000218 High palate
HP:0001305 Dandy-Walker malformation
HP:0000494 Downslanted palpebral fissures
HP:0000270 Delayed cranial suture closure
HP:0001249 Intellectual disability
HP:0000691 Microdontia
HP:0000308 Microretrognathia
HP:0001511 Intrauterine growth retardation
HP:0000007 Autosomal recessive inheritance
Displaying 1 entry
Gene ID Gene Symbol Description
23545 ATP6V0A2 ATPase H+ transporting V0 subunit a2

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Last updated: December 9, 2024