Syndromic X-linked intellectual disability type 7

disorder

SNOMED 719160009CUI C1846170

Overview

Syndromic X-linked intellectual disability type 7 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.

Decreased activity of gonads

Very frequent (80-99%)HP:0000135

Mental-retardation

Very frequent (80-99%)HP:0001249

Moderate mental retardation

Very frequent (80-99%)HP:0002342

Obesity

Very frequent (80-99%)HP:0001513

Tapering fingers

Very frequent (80-99%)HP:0001182

Decreased body height

Frequent (30-79%)HP:0004322

Hypoplasia of penis

Frequent (30-79%)HP:0008736

Incomprehensible speech

Frequent (30-79%)HP:0002546

Misalignment of teeth

Frequent (30-79%)HP:0000692

Misshapened teeth

Frequent (30-79%)HP:0006482

Muscle weakness

Frequent (30-79%)HP:0001324

Sparse body hair

Frequent (30-79%)HP:0002231

Cryptorchidism

Occasional (5-29%)HP:0000028

Short penis

Occasional (5-29%)HP:0000054

Visual loss

Occasional (5-29%)HP:0000572

Related Conditions

Hypogonadism(parent)

Hereditary disorder of endocrine system(parent)

Reproductive system hereditary disorder(parent)

Congenital disease(parent)

Developmental hereditary disorder(parent)

X-linked recessive hereditary disease(parent)

Genetic obesity disorder(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 719160009
UMLS CUI: C1846170
Fully Specified Name: Syndromic X-linked intellectual disability type 7 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.