Fetal hydantoin syndrome
ICD-10: Q86.1MeSH: C537922ORPHA: 1912
Overview
medical condition
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Fetal hydantoin syndrome, sourced from HPO and Orphanet clinical annotations.
Hearing abnormalityAbnormal pinna morphologyDepressed nasal ridgeShort noseAbnormal dermatoglyphicsBifid scrotumWide mouthEverted lower lip vermilionAbnormal cranial suture/fontanelle morphologyMicrocephalyEpicanthusHypertelorismThickened nuchal skin foldStrabismusPtosisTriphalangeal thumbGlobal developmental delayIntrauterine growth retardationHypoplastic fingernailLow posterior hairlineCoarse hairShort statureWide intermamillary distanceShort distal phalanx of fingerHerniaCryptorchidismCleft palateAbnormality of the cardiovascular systemNeoplasmPosteriorly rotated ears
Classification & Codes
ICD-10 Code
Q86.1MeSH Code
C537922Orphanet Code
ORPHA:1912Fetal hydantoin syndrome
| ICD-10 | Q86.1 |
| MeSH | C537922 |
| Orphanet | ORPHA:1912 |
| Treatments | 0 drug(s) |
| Symptoms on record | 30 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO