Fetal hydantoin syndrome

disorder

SNOMED 70065001CUI C0265372

Overview

Fetal hydantoin 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 dermatoglyphics

Very frequent (80-99%)HP:0007477

Dysplastic ears

Very frequent (80-99%)HP:0000377

Hearing abnormality

Very frequent (80-99%)HP:0000364

Nasal hypoplasia

Very frequent (80-99%)HP:0003196

Posteriorly angulated ears

Very frequent (80-99%)HP:0000358

Retruded nasal dorsum

Very frequent (80-99%)HP:0000457

Abnormal cranial suture/fontanelle morphology

Frequent (30-79%)HP:0000235

Decreased body height

Frequent (30-79%)HP:0004322

Decreased size of cranium

Frequent (30-79%)HP:0000252

Distal phalangeal hypoplasia

Frequent (30-79%)HP:0009882

Eclabium of lower lip

Frequent (30-79%)HP:0000232

Eye drop

Frequent (30-79%)HP:0000508

Hernia

Frequent (30-79%)HP:0100790

Increased distance between eyes

Frequent (30-79%)HP:0000316

Intrauterine growth retardation, IUGR

Frequent (30-79%)HP:0001511

Large mouth

Frequent (30-79%)HP:0000154

Low posterior hair line

Frequent (30-79%)HP:0002162

Mental and motor retardation

Frequent (30-79%)HP:0001263

Palpebronasal fold

Frequent (30-79%)HP:0000286

Rough hair texture

Frequent (30-79%)HP:0002208

Scrotal cleft

Frequent (30-79%)HP:0000048

Small fingernail

Frequent (30-79%)HP:0001804

Squint

Frequent (30-79%)HP:0000486

Thickened skin folds of neck

Frequent (30-79%)HP:0000474

Triphalangy of thumb

Frequent (30-79%)HP:0001199

Wide-spaced nipples

Frequent (30-79%)HP:0006610

Abnormal tissue mass

Occasional (5-29%)HP:0002664

Abnormality of the cardiovascular system

Occasional (5-29%)HP:0001626

Cleft of palate

Occasional (5-29%)HP:0000175

Cryptorchidism

Occasional (5-29%)HP:0000028

Related Conditions

Disorder of foetal structure(parent)

Foetal disorder caused by chemicals(parent)

Quick Facts

SNOMED CT: 70065001
UMLS CUI: C0265372
Fully Specified Name: Fetal hydantoin 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.