Limb body wall complex

disorder

SNOMED 716106000CUI C4274839

Overview

Limb body wall complex 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 insertion of umbilical cord

Very frequent (80-99%)HP:0011418

Congenital anterior abdominal wall defect

Very frequent (80-99%)HP:0010866

Limb anomaly

Very frequent (80-99%)HP:0040064

Abnormality of the backbone

Frequent (30-79%)HP:0000925

Abnormality of the chest

Frequent (30-79%)HP:0000765

Aplasia/Hypoplasia involving bones of the thorax

Frequent (30-79%)HP:0006711

Atria septal defect

Frequent (30-79%)HP:0001631

Cardiac anomaly

Frequent (30-79%)HP:0001627

Diaphragmatic hernia

Frequent (30-79%)HP:0000776

Ectopia cordis

Frequent (30-79%)HP:0001683

Morphological abnormality of the CNS

Frequent (30-79%)HP:0002011

Renal anomalies

Frequent (30-79%)HP:0000077

Short umbilical cord

Frequent (30-79%)HP:0001196

Thoracic hypoplasia

Frequent (30-79%)HP:0005257

VSD

Frequent (30-79%)HP:0001629

2 vessel cord

Occasional (5-29%)HP:0001195

Abnormal spinal cord morphology

Occasional (5-29%)HP:0002143

Abnormality of the intestine

Occasional (5-29%)HP:0002242

Absent proximal phalanges

Occasional (5-29%)HP:0010242

Amniotic constriction band

Occasional (5-29%)HP:0009775

Aplasia/hypoplasia involving bones of the upper limbs

Occasional (5-29%)HP:0006496

Bifid skull

Occasional (5-29%)HP:0002084

Bilateral clubfeet

Occasional (5-29%)HP:0001776

Broad big toe

Occasional (5-29%)HP:0010055

Choanal atresia

Occasional (5-29%)HP:0000453

Cleft lip

Occasional (5-29%)HP:0410030

Cleft of palate

Occasional (5-29%)HP:0000175

Corneal opacity

Occasional (5-29%)HP:0007957

Duplication of hand bones

Occasional (5-29%)HP:0004275

Fetal anencephaly

Occasional (5-29%)HP:0002323

Related Conditions

Multiple malformation syndrome with limb defect as major feature(parent)

Congenital anomaly of body wall(parent)

Congenital anomaly of lower trunk(parent)

Quick Facts

SNOMED CT: 716106000
UMLS CUI: C4274839
Fully Specified Name: Limb body wall complex (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.