Congenital constriction band

disorder

SNOMED 765206003CUI C0002636

Overview

Congenital constriction band 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.

Abnormal hair whorl

Frequent (30-79%)HP:0010721

Abnormality of the lower limb

Frequent (30-79%)HP:0002814

Amniotic constriction band

Frequent (30-79%)HP:0009775

Amniotic constriction rings of legs

Frequent (30-79%)HP:0010495

Bulging forehead

Frequent (30-79%)HP:0011220

Digital constriction ring

Frequent (30-79%)HP:0010491

Increased distance between eyes

Frequent (30-79%)HP:0000316

Nonsyndromal hydrocephalus

Frequent (30-79%)HP:0000238

Abnormality of the arm

Occasional (5-29%)HP:0002817

Amniotic constriction rings of arms

Occasional (5-29%)HP:0010483

Bifid skull

Occasional (5-29%)HP:0002084

Cleft lip

Occasional (5-29%)HP:0410030

Cleft of palate

Occasional (5-29%)HP:0000175

Cobb angle greater than ten degrees

Occasional (5-29%)HP:0002650

Congenital joint contractures

Occasional (5-29%)HP:0002803

Craniofacial cleft

Occasional (5-29%)HP:5201015

Ectopia cordis

Occasional (5-29%)HP:0001683

Edema of the upper limbs

Occasional (5-29%)HP:0010742

Feeding difficulties in infancy

Occasional (5-29%)HP:0008872

Foot, talipes equinovarus

Occasional (5-29%)HP:0001762

Gastroschisis

Occasional (5-29%)HP:0001543

Hypoplastic or absent corpus callosum

Occasional (5-29%)HP:0007370

Less than 10 fetal movements in 12 hours

Occasional (5-29%)HP:0001558

Mental and motor retardation

Occasional (5-29%)HP:0001263

Notched pupil

Occasional (5-29%)HP:0000589

Omphalocoele

Occasional (5-29%)HP:0001539

Pedal oedema

Occasional (5-29%)HP:0010741

Premature birth

Occasional (5-29%)HP:0001622

Related Conditions

Constricting band of extremity(child)

Congenital deformity(parent)

Quick Facts

SNOMED CT: 765206003
UMLS CUI: C0002636
Fully Specified Name: Constriction ring syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

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.