Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Bardet-Biedl syndrome
Occasional (5-29%)
Familial amyloid polyneuropathy, Iowa type
Always present (100%)
African trypanosomiasis
Occasional (5-29%)
Ring chromosome 21 syndrome
Frequent (30-79%)
XXXXY syndrome
Very frequent (80-99%)
Asherman syndrome
Occasional (5-29%)
Testosterone 17-beta-dehydrogenase deficiency
Very frequent (80-99%)
Juvenile hemochromatosis
Isolated prolactin deficiency
Rothmund-Thomson syndrome
Frequent (30-79%)
Acromegaly
Occasional (5-29%)
XXXY syndrome
Very frequent (80-99%)
Trypanosomiasis
Occasional (5-29%)
Wilson's disease
Occasional (5-29%)
Prader-Willi syndrome
Very frequent (80-99%)
Idiopathic hypogonadotropic hypogonadism
Occasional (5-29%)
Westphal-Strumpell syndrome
Occasional (5-29%)
Post-traumatic hypopituitarism
Occasional (5-29%)
Axial osteosclerosis
Thyrotroph adenoma
Occasional (5-29%)
Gonadotrophin-secreting pituitary adenoma
Frequent (30-79%)
XXYY syndrome
Very frequent (80-99%)
Der(22) syndrome due to 3:1 meiotic disjunction events
Frequent (30-79%)
Isochromosome 9p
Occasional (5-29%)
Left renal vein entrapment syndrome
Very rare (1-4%)
Related Symptoms
Quick Facts
- SNOMED CT
- 8619003
- UMLS CUI
- C0021359
- Fully Specified Name
- Infertile (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.