X-linked intellectual disability Atkin type

disorder

SNOMED 718577005CUI C0796206

Overview

X-linked intellectual disability Atkin type 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

Coarse face

Very frequent (80-99%)HP:0000280

Decreased body height

Very frequent (80-99%)HP:0004322

Dental problems

Very frequent (80-99%)HP:0000164

Eclabium of lower lip

Very frequent (80-99%)HP:0000232

Hypertrophy of supraorbital margins

Very frequent (80-99%)HP:0000336

Hypotrophic maxillary lateral incisor

Very frequent (80-99%)HP:0001593

Increased size of skull

Very frequent (80-99%)HP:0000256

Increased width of the forehead

Very frequent (80-99%)HP:0000337

Large testis

Very frequent (80-99%)HP:0000053

Nostrils anteverted

Very frequent (80-99%)HP:0000463

Obesity

Very frequent (80-99%)HP:0001513

Poor school performance

Very frequent (80-99%)HP:0001249

Prominent lips

Very frequent (80-99%)HP:0012471

Increased distance between eyes

Frequent (30-79%)HP:0000316

Large pinnae

Frequent (30-79%)HP:0000400

Related Conditions

Small stature(parent)

Developmental hereditary disorder(parent)

Congenital macrocephaly(parent)

X-linked dominant hereditary disease(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 718577005
UMLS CUI: C0796206
Fully Specified Name: X-linked intellectual disability Atkin type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.