Ring chromosome 11 syndrome

disorder

SNOMED 111310003CUI C0265444

Overview

Ring chromosome 11 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.

Anomaly of the face

Frequent (30-79%)HP:0000271

Birthmark

Frequent (30-79%)HP:0000957

Decreased body height

Frequent (30-79%)HP:0004322

Decreased size of cranium

Frequent (30-79%)HP:0000252

Low body weight

Frequent (30-79%)HP:0004325

Low intelligence

Frequent (30-79%)HP:0001249

Psychomotor development deficiency

Frequent (30-79%)HP:0001263

Cardiac anomaly

Occasional (5-29%)HP:0001627

Cryptorchidism

Occasional (5-29%)HP:0000028

Curvature of digit

Occasional (5-29%)HP:0030084

Hirsutism

Occasional (5-29%)HP:0001007

Hypospadias

Occasional (5-29%)HP:0000047

Hypothyroidism

Occasional (5-29%)HP:0000821

Intrauterine growth retardation, IUGR

Occasional (5-29%)HP:0001511

Nephroblastoma

Occasional (5-29%)HP:0002667

Obesity

Occasional (5-29%)HP:0001513

Patchy hypopigmentation

Occasional (5-29%)HP:0005590

Precocious puberty

Occasional (5-29%)HP:0000826

Prominent clitoris

Occasional (5-29%)HP:0008665

Retarded growth

Occasional (5-29%)HP:0001510

Speech difficulties

Occasional (5-29%)HP:0000750

Related Conditions

Anomaly of chromosome pair 11(parent)

Ring chromosome(parent)

Multiple system malformation syndrome(parent)

Quick Facts

SNOMED CT: 111310003
UMLS CUI: C0265444
Fully Specified Name: Ring chromosome 11 syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 21

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.