alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
MeSH: C563370ORPHA: 1014
Overview
This syndrome is characterized by the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism
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 alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome, sourced from HPO and Orphanet clinical annotations.
Hypergonadotropic hypogonadismMild intellectual disabilityAlopecia totalis
Classification & Codes
MeSH Code
C563370Orphanet Code
ORPHA:1014alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome
| MeSH | C563370 |
| Orphanet | ORPHA:1014 |
| Treatments | 0 drug(s) |
| Symptoms on record | 3 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO