Frank–Ter Haar syndrome
MeSH: C537274ORPHA: 137834
Overview
human disease
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 Frank–Ter Haar syndrome, sourced from HPO and Orphanet clinical annotations.
Wide mouthCoarse facial featuresHypertelorismShort philtrumWide nasal bridgeDeeply set eyeAcneThickened skinBrachydactylyMitral valve prolapseOsteolysisDepressed nasal bridgeAvascular necrosisThick vermilion borderGingival overgrowthMandibular prognathiaBroad foreheadHigh foreheadProtruding earDownslanted palpebral fissuresDelayed eruption of teethJoint stiffnessScoliosisKyphosisGenu recurvatumClinodactyly of the 5th fingerBeaking of vertebral bodiesAbnormal metacarpal morphologyPremature loss of teethCamptodactyly of fingerInguinal herniaGynecomastiaUmbilical hernia
Classification & Codes
MeSH Code
C537274Orphanet Code
ORPHA:137834Frank–Ter Haar syndrome
| MeSH | C537274 |
| Orphanet | ORPHA:137834 |
| Treatments | 0 drug(s) |
| Symptoms on record | 33 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO