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XXXY syndrome

disorder
SNOMED 78317008CUI C0265498

Overview

By MedlinePlus, National Library of Medicine

NIH: National Institute of Child Health and Human Development Courtesy of the National Library of Medicine. Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Azoospermia
Very frequent (80-99%)HP:0000027
Decreased activity of gonads
Very frequent (80-99%)HP:0000135
Decreased testicular size
Very frequent (80-99%)HP:0008734
Infertility
Very frequent (80-99%)HP:0000789
Language impairment
Very frequent (80-99%)HP:0002463
Mental retardation, mild
Very frequent (80-99%)HP:0001256
Psychomotor development deficiency
Very frequent (80-99%)HP:0001263
Accelerated linear growth
Frequent (30-79%)HP:0000098
Anomaly of the epiphyses
Frequent (30-79%)HP:0005930
Autism
Frequent (30-79%)HP:0000717
Bronchial asthma
Frequent (30-79%)HP:0002099
Central hypotonia
Frequent (30-79%)HP:0001252
Childhood attention deficit/hyperactivity disorder
Frequent (30-79%)HP:0007018
Chronic middle ear infection
Frequent (30-79%)HP:0000389
Constipation
Frequent (30-79%)HP:0002019
Cryptorchidism
Frequent (30-79%)HP:0000028
Delayed eruption of teeth
Frequent (30-79%)HP:0000684
Dental cavities
Frequent (30-79%)HP:0000670
Dropped arches
Frequent (30-79%)HP:0001763
Dystrophic tooth enamel
Frequent (30-79%)HP:0000682
Fused forearm bones
Frequent (30-79%)HP:0002974
Gynaecomastia
Frequent (30-79%)HP:0000771
Hypoplasia of penis
Frequent (30-79%)HP:0008736
Increased distance between eyes
Frequent (30-79%)HP:0000316
Joint ligamentous laxity
Frequent (30-79%)HP:0001382
Large elongated pulp chamber
Frequent (30-79%)HP:0000679
Mongoloid slant
Frequent (30-79%)HP:0000582
Open bite
Frequent (30-79%)HP:0010807
Palpebronasal fold
Frequent (30-79%)HP:0000286
Permanent curving of the pinkie finger
Frequent (30-79%)HP:0004209

Quick Facts

SNOMED CT
78317008
UMLS CUI
C0265498
Fully Specified Name
XXXY 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.