WSS - Wrinkly skin syndrome

disorder

SNOMED 238875009CUI C0406587

Overview

WSS - Wrinkly skin syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Excessive skin wrinkling on back of hands and fingers

Always present (100%)HP:0007407

Grey sclerae

Always present (100%)HP:0000592

Loose redundant skin

Always present (100%)HP:0001582

Muscular ventricular septal defect

Always present (100%)HP:0011623

Progeroid facial appearance

Always present (100%)HP:0005328

Retromicrognathia

Always present (100%)HP:0000308

Scaphocephaly

Always present (100%)HP:0030799

Abnormality of the cheek

Very frequent (80-99%)HP:0004426

Broad, upturned nose

Very frequent (80-99%)HP:0000455

Congenital hip dislocations

Very frequent (80-99%)HP:0001374

Decreased muscle mass

Very frequent (80-99%)HP:0003199

Deep nasolabial crease

Very frequent (80-99%)HP:0005272

Deep palmar creases

Very frequent (80-99%)HP:0006191

Delayed eruption of teeth

Very frequent (80-99%)HP:0000684

Down-slanting palpebral fissure

Very frequent (80-99%)HP:0000494

Dropped arches

Very frequent (80-99%)HP:0001763

Excessive wrinkled skin

Very frequent (80-99%)HP:0007392

Extra bones within cranial sutures

Very frequent (80-99%)HP:0002645

Fragmented elastic fibers in the dermis

Very frequent (80-99%)HP:0025167

Generalized joint laxity

Very frequent (80-99%)HP:0002761

Growth delay as children

Very frequent (80-99%)HP:0008897

Hanging skin

Very frequent (80-99%)HP:0000973

High arched palate

Very frequent (80-99%)HP:0000218

High nonceruloplasmin-bound serum copper

Very frequent (80-99%)HP:0010838

Hypotonia, early

Very frequent (80-99%)HP:0008947

Inability to make and keep healthy fat tissue

Very frequent (80-99%)HP:0009125

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Increased length of philtrum

Very frequent (80-99%)HP:0000343

Inguinal hernia

Very frequent (80-99%)HP:0000023

Intrauterine growth retardation, IUGR

Very frequent (80-99%)HP:0001511

Related Conditions

Premature ageing syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Congenital anomaly of skin(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 238875009
UMLS CUI: C0406587
Fully Specified Name: Wrinkly skin syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.