OMOP Concept 45757367
Partial androgen insensitivity syndrome
StandardConditionSNOMED122811000119101Disorder
Maps from
7
Descendants
2
Valid from
31 Jan 2015
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Partial androgen insensitivity syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 113366 | Hereditary familial hypogonadism with hypospadias and gynecomastia | Non-standard |
| CIEL | 137610 | Incomplete testicular feminization syndrome | Non-standard |
| ICD10CM | E34.52 | Partial androgen insensitivity syndrome | Non-standard |
| ICD9CM | 259.52 | Partial androgen insensitivity | Non-standard |
| Nebraska Lexicon | 122811000119101 | Partial androgen insensitivity syndrome | Non-standard |
| Nebraska Lexicon | 58672003 | Familial incomplete male pseudohermaphroditism, type 1 | Non-standard |
| Nebraska Lexicon | 67528009 | Incomplete testicular feminisation syndrome | Non-standard |
Synonyms
Alternative names recorded for Partial androgen insensitivity syndrome across source vocabularies.
- Familial incomplete male pseudohermaphroditism type 1
- PAIS - partial androgen insensitivity syndrome
- Partial androgen insensitivity syndrome (disorder)
- Partial androgen resistance syndrome
- pseudohermafroditismo masculino incompleto familiar tipo 1
- Reifenstein syndrome
- síndrome de insensibilidad androgénica parcial
- síndrome de insensibilidad androgénica parcial (trastorno)
- síndrome de insensibilidad parcial a andrógenos
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Androgen resistance syndrome
- 1Male pseudohermaphroditism
- 246,XY disorder of sex development
- 2Congenital anomaly of endocrine gonad
- 2Developmental hereditary disorder
- 2Disorder of androgen receptor
- 2Disorder of pelvic region of trunk
- 2Hereditary disorder of endocrine system
- 2Pseudohermaphroditism
- 2Reproductive system hereditary disorder
- 2X-linked recessive hereditary disease
- 3Congenital anomaly of endocrine gland
- 3Congenital malformation of genital organs
- 3Developmental disorder
- 3Disorder of abdominopelvic segment of trunk
- 3Disorder of endocrine gonad
- 3Disorder of endocrine receptor
- 3Disorder of endocrine system
- 3Disorder of reproductive system
- 3Disorder of steroid metabolism
- 3Endocrine andrology disorder
- 3Finding of pelvic region of trunk
- 3Gonadal dysgenesis
- 3Hereditary disease
- 3Hereditary disorder by system
Narrower concepts
(2)Included automatically when you query with descendants.
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