Craniorachischisis

disorder

SNOMED 32219008CUI C0152426

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Cervical spina bifida

Very frequent (80-99%)HP:0005857

Fetal anencephaly

Very frequent (80-99%)HP:0002323

Incomplete closure of the vertebral arch

Very frequent (80-99%)HP:0010301

Myelomeningocele

Very frequent (80-99%)HP:0002475

Absent anus

Occasional (5-29%)HP:0002023

Diaphragmatic hernia

Occasional (5-29%)HP:0000776

Omphalocoele

Occasional (5-29%)HP:0001539

Sternal cleft

Occasional (5-29%)HP:0010309

Sympodia

Occasional (5-29%)HP:0010497

Related Conditions

Iniencephaly(child)

Neural tube defect(parent)

Quick Facts

SNOMED CT: 32219008
UMLS CUI: C0152426
Fully Specified Name: Craniorachischisis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.