Overview
Congenital hypogonadotropic hypogonadism is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome(child)
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome(child)
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome(child)
Hypogonadism with anosmia(child)
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome(child)
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome(child)
Prader-Willi-like syndrome(child)
ANE syndrome(child)
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome(child)
Familial adrenal hypoplasia with absent pituitary luteinizing hormone(child)
Obesity due to leptin receptor gene deficiency(child)
Prader-Willi syndrome(child)
Chudley Rozdilsky syndrome(child)
Congenital leptin deficiency(child)
Hypogonadotropic hypogonadism(parent)
Congenital disease(parent)
Quick Facts
- SNOMED CT
- 722944006
- UMLS CUI
- C3899503
- Fully Specified Name
- Congenital hypogonadotropic hypogonadism (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.