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Wilson Turner syndrome

disorder
SNOMED 719834005CUI C1839736

Overview

Wilson Turner 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.

Broad, upturned nose
Very frequent (80-99%)HP:0000455
Cognitive delay
Very frequent (80-99%)HP:0001263
Cryptorchidism
Very frequent (80-99%)HP:0000028
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased volume of upper lip
Very frequent (80-99%)HP:0000219
Deep set eye
Very frequent (80-99%)HP:0000490
Difficulty speaking
Very frequent (80-99%)HP:0002465
Disproportionately small hands
Very frequent (80-99%)HP:0200055
Distortion of face
Very frequent (80-99%)HP:0001999
Emotional lability
Very frequent (80-99%)HP:0000712
Fallen arches
Very frequent (80-99%)HP:0001763
Gynaecomastia
Very frequent (80-99%)HP:0000771
Hyperplasia of supraorbital ridge
Very frequent (80-99%)HP:0000336
Hypoplastic mandible condyle
Very frequent (80-99%)HP:0000347
Malar hyperplasia
Very frequent (80-99%)HP:0010620
Microtia
Very frequent (80-99%)HP:0008551
Obesity
Very frequent (80-99%)HP:0001513
Pes cavus
Very frequent (80-99%)HP:0001761
Poor school performance
Very frequent (80-99%)HP:0001249
Small feet
Very frequent (80-99%)HP:0001773
Tapering fingers
Very frequent (80-99%)HP:0001182
Thick eyebrow
Very frequent (80-99%)HP:0000574
Truncal obesity
Very frequent (80-99%)HP:0001956
Isolated hypogonadotropic hypogonadism
Frequent (30-79%)HP:0000044
Stuttering
Frequent (30-79%)HP:0025268
Decreased size of cranium
Occasional (5-29%)HP:0000252
Nonverbal
Occasional (5-29%)HP:0001344
Seizures
Occasional (5-29%)HP:0001250
Specific learning disability
Occasional (5-29%)HP:0001328
Delayed language development
HP:0000750

Related Conditions

Multiple malformation syndrome with facial defects as major feature(parent)
X-linked hereditary disease(parent)
Centripetal obesity(parent)
Developmental hereditary disorder(parent)
Genetic obesity disorder(parent)
Genetic intellectual disability(parent)

Quick Facts

SNOMED CT
719834005
UMLS CUI
C1839736
Fully Specified Name
Wilson Turner 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.