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48,XYYY syndrome

disorder
SNOMED 733625003CUI C4518082

Overview

48,XYYY 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.

Abnormal dermatoglyphics
Very frequent (80-99%)HP:0007477
Abnormality of the feet
Very frequent (80-99%)HP:0001760
Accelerated linear growth
Very frequent (80-99%)HP:0000098
Azoospermia
Very frequent (80-99%)HP:0000027
Behavioural/Psychiatric abnormality
Very frequent (80-99%)HP:0000708
Breaking out
Very frequent (80-99%)HP:0001061
Cognitive delay
Very frequent (80-99%)HP:0001263
Concave bridge of nose
Very frequent (80-99%)HP:0005280
Decreased function of male gonad
Very frequent (80-99%)HP:0000026
Enamel dysplasia
Very frequent (80-99%)HP:0006297
Fallen arches
Very frequent (80-99%)HP:0001763
Feeding difficulties
Very frequent (80-99%)HP:0011968
Full lower lip
Very frequent (80-99%)HP:0000179
Fused forearm bones
Very frequent (80-99%)HP:0002974
High arched palate
Very frequent (80-99%)HP:0000218
Impulsivity
Very frequent (80-99%)HP:0100710
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Increased length of philtrum
Very frequent (80-99%)HP:0000343
Intolerance to frustration
Very frequent (80-99%)HP:0000744
Kidney malformation
Very frequent (80-99%)HP:0012210
Mental retardation, mild
Very frequent (80-99%)HP:0001256
Mental-retardation
Very frequent (80-99%)HP:0001249
Palpebronasal fold
Very frequent (80-99%)HP:0000286
physical aggression
Very frequent (80-99%)HP:0000718
Primary gonadal insufficiency
Very frequent (80-99%)HP:0008193
Radial head dislocation
Very frequent (80-99%)HP:0003083
Reactive airway disease
Very frequent (80-99%)HP:0002099
Recurrent URI
Very frequent (80-99%)HP:0002788
Short neck
Very frequent (80-99%)HP:0000470
Speech and language difficulties
Very frequent (80-99%)HP:0000750

Related Conditions

Anomaly of chromosome Y(parent)
Sex chromosome abnormality - male phenotype(parent)
Multiple system malformation syndrome(parent)
Sex chromosome aneuploidy(parent)

Quick Facts

SNOMED CT
733625003
UMLS CUI
C4518082
Fully Specified Name
48,XYYY 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.