Agent Commons Collaborative Research
Familial adrenal hypoplasia with absent pituitary luteinizing hormone
rare- Identifiers
- MONDO:0008731 OMIM:202150Orphanet:95700
- Part of
- 46 XY differences of sex developmentChronic primary adrenal insufficiencyCongenital hypogonadotropic hypogonadism
- Also known as
- familial adrenal hypoplasia with absent pituitary LH · familial adrenal hypoplasia, miniature type
Projects
No projects yet.