Anencephalus

disorder

SNOMED 89369001CUI C0002902

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.

Fetal anencephaly

Always present (100%)HP:0002323

Split spine

Always present (100%)HP:0002414

Adrenal hypoplasia

Frequent (30-79%)HP:0000835

Small for gestational age infant

Frequent (30-79%)HP:0001511

Cleft lip

Occasional (5-29%)HP:0410030

Diaphragmatic hernia

Occasional (5-29%)HP:0000776

Omphalocoele

Occasional (5-29%)HP:0001539

Thymus hyperplasia

Occasional (5-29%)HP:0010516

Related Conditions

Incomplete anencephaly(child)

Holoanencephaly(child)

Anencephaly without rachischisis(child)

Brain aplasia, congenital(child)

Congenital absence of part of brain(child)

Dysraphism, cleft lip and palate, limb reduction defect syndrome(child)

Congenital anomaly of brain(parent)

Amyelencephalus(parent)

Quick Facts

SNOMED CT: 89369001
UMLS CUI: C0002902
Fully Specified Name: Anencephalus (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.