Ring chromosome 15 syndrome

disorder

SNOMED 763405000CUI C0795855

Overview

Ring chromosome 15 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.

Decreased body height

Very frequent (80-99%)HP:0004322

Birth length less than 3rd percentile

Frequent (30-79%)HP:0003561

Birth weight less than 10th percentile

Frequent (30-79%)HP:0001518

Clinodactyly

Frequent (30-79%)HP:0030084

Cognitive delay

Frequent (30-79%)HP:0001263

Decreased size of cranium

Frequent (30-79%)HP:0000252

Delayed skeletal development

Frequent (30-79%)HP:0002750

Feeding difficulties in infancy

Frequent (30-79%)HP:0008872

Genitourinary disease

Frequent (30-79%)HP:0000119

Growth failure

Frequent (30-79%)HP:0001510

Inverted triangular face

Frequent (30-79%)HP:0000325

Low intelligence

Frequent (30-79%)HP:0001249

Small for gestational age infant

Frequent (30-79%)HP:0001511

Brachydactyly

Occasional (5-29%)HP:0001156

Broad flat nasal bridge

Occasional (5-29%)HP:0000431

Cardiac anomaly

Occasional (5-29%)HP:0001627

Cobb angle greater than ten degrees

Occasional (5-29%)HP:0002650

Cryptorchidism

Occasional (5-29%)HP:0000028

Delayed language development

Occasional (5-29%)HP:0000750

Disproportionately small hands

Occasional (5-29%)HP:0200055

Downturned corners of mouth

Occasional (5-29%)HP:0002714

Foot, talipes equinovarus

Occasional (5-29%)HP:0001762

Frontal protuberance

Occasional (5-29%)HP:0002007

Hunched back

Occasional (5-29%)HP:0002808

Hypoplastic mandible

Occasional (5-29%)HP:0000347

Hypospadias

Occasional (5-29%)HP:0000047

Increased distance between eyes

Occasional (5-29%)HP:0000316

Narrow, high-arched roof of mouth

Occasional (5-29%)HP:0002705

Oligospermia

Occasional (5-29%)HP:0000798

Peripheral hypotonia

Occasional (5-29%)HP:0001252

Related Conditions

Anomaly of chromosome pair 15(parent)

Ring chromosome(parent)

Multiple system malformation syndrome(parent)

Quick Facts

SNOMED CT: 763405000
UMLS CUI: C0795855
Fully Specified Name: Ring chromosome 15 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.