Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Absent facial hair
HP:0002550
Blind-ended vagina
HP:0040314
Decreased sexual hair
HP:0002225
Elevated circulating follicle stimulating hormone level
HP:0008232
Elevated circulating luteinizing hormone level
HP:0011969
Female external genitalia in individual with 46,XY karyotype
HP:0008730
Growth abnormality
HP:0001507
Gynaecomastia
HP:0000771
Hypoplastic labia
HP:0000066
Inguinal hernia
HP:0000023
Oncology
HP:0002664
Primary amenorrhea
HP:0000786
sparse to absent axillary hair
HP:0002215
Related Conditions
Complete androgen insensitivity syndrome(child)
Partial androgen insensitivity syndrome(child)
Testicular lesion in androgen insensitivity syndrome(child)
Stromal cell hyperplasia in androgen insensitivity syndrome(child)
Disorder of androgen receptor(parent)
X-linked recessive hereditary disease(parent)
Developmental hereditary disorder(parent)
Hereditary disorder of endocrine system(parent)
Reproductive system hereditary disorder(parent)
Congenital anomaly of endocrine gonad(parent)
46,XY disorder of sex development(parent)
Quick Facts
- SNOMED CT
- 12313004
- UMLS CUI
- C0039585
- Fully Specified Name
- Androgen resistance syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 13
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.