Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased circulating follicle stimulating hormone concentration
Always present (100%)HP:0030341
Decreased circulating luteinizing hormone level
Always present (100%)HP:0030344
Decreased testosterone
Always present (100%)HP:0040171
Abnormal erection
Very frequent (80-99%)HP:0100639
Anterior hypopituitarism
Very frequent (80-99%)HP:0000830
Decreased fertility
Very frequent (80-99%)HP:0000144
Decreased testicular size
Very frequent (80-99%)HP:0008734
Delayed puberty
Very frequent (80-99%)HP:0000823
Hypoplasia of penis
Very frequent (80-99%)HP:0008736
Hypothalamic GNRH deficiency
Very frequent (80-99%)HP:0003164
Lost smell
Very frequent (80-99%)HP:0000458
Low gonadotropins (secondary hypogonadism)
Very frequent (80-99%)HP:0000044
Sense of smell impaired
Very frequent (80-99%)HP:0004409
Short penis
Very frequent (80-99%)HP:0000054
Cryptorchidism
Frequent (30-79%)HP:0000028
Decreased bone mineral density Z score
Frequent (30-79%)HP:0004349
Smaller than typical growth of scrotum
Frequent (30-79%)HP:0000046
Underdeveloped breasts
Frequent (30-79%)HP:0003187
Voice abnormality
Frequent (30-79%)HP:0001608
Abnormal colour vision
Occasional (5-29%)HP:0000551
Abnormal morphology of female internal genitalia
Occasional (5-29%)HP:0000008
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
Ataxia
Occasional (5-29%)HP:0001251
Cavus foot
Occasional (5-29%)HP:0001761
Central hypotonia
Occasional (5-29%)HP:0001252
Cleft of palate
Occasional (5-29%)HP:0000175
Dental agenesis
Occasional (5-29%)HP:0009804
Difficulty articulating speech
Occasional (5-29%)HP:0001260
Dyspareunia
Occasional (5-29%)HP:0030016
Epilepsy
Occasional (5-29%)HP:0001250
Related Conditions
Kallman syndrome with heart disease(child)
Disorder of olfactory system(parent)
Multiple system malformation syndrome(parent)
Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency(parent)
Congenital hypogonadotropic hypogonadism(parent)
Genetic disease(parent)
Congenital anomaly of nervous system(parent)
Quick Facts
- SNOMED CT
- 93559003
- UMLS CUI
- C0162809
- Fully Specified Name
- Hypogonadism with anosmia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.