Fetal aminopterin syndrome

disorder

SNOMED 65986000CUI C0432367

Overview

Fetal aminopterin 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.

Abnormal skeletal development

Very frequent (80-99%)HP:0002652

Broad flat nasal bridge

Very frequent (80-99%)HP:0000431

Decreased body height

Very frequent (80-99%)HP:0004322

Fetal anencephaly

Very frequent (80-99%)HP:0002323

Hypertrophy of mandible

Very frequent (80-99%)HP:0000303

Hypoplasia of supraorbital margins

Very frequent (80-99%)HP:0009891

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Mesomelia

Very frequent (80-99%)HP:0003027

Micromelia

Very frequent (80-99%)HP:0002983

Nonsyndromal hydrocephalus

Very frequent (80-99%)HP:0000238

Palpebronasal fold

Very frequent (80-99%)HP:0000286

Prominent globes

Very frequent (80-99%)HP:0000520

Bifid skull

Frequent (30-79%)HP:0002084

Cleft of palate

Frequent (30-79%)HP:0000175

Decreased size of cranium

Frequent (30-79%)HP:0000252

Hypoplastic mandible condyle

Frequent (30-79%)HP:0000347

Intrauterine growth retardation, IUGR

Frequent (30-79%)HP:0001511

Meningocele

Frequent (30-79%)HP:0002435

Non-midline cleft of the upper lip

Frequent (30-79%)HP:0100335

Posteriorly angulated ears

Frequent (30-79%)HP:0000358

Talipes

Frequent (30-79%)HP:0001883

Abnormality of the fingernails

Occasional (5-29%)HP:0001231

Aplastic/hypoplastic thumbs

Occasional (5-29%)HP:0009601

Atresia of the pulmonary artery

Occasional (5-29%)HP:0004935

Cerebellar hypoplasia/atrophy

Occasional (5-29%)HP:0007360

Hypoplastic or absent corpus callosum

Occasional (5-29%)HP:0007370

Incomplete closure of the vertebral arch

Occasional (5-29%)HP:0010301

Partial syndactyly

Occasional (5-29%)HP:0006101

Single brain ventricle

Occasional (5-29%)HP:0001360

Situs inversus

Occasional (5-29%)HP:0001696

Related Conditions

Fetus with drug damage(parent)

Disorder of foetal structure(parent)

Foetal disorder caused by chemicals(parent)

Quick Facts

SNOMED CT: 65986000
UMLS CUI: C0432367
Fully Specified Name: Fetal aminopterin 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.