OMOP Concept 37110899
Autosomal recessive facio-digito-genital syndrome
StandardConditionSNOMED725434009Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Autosomal recessive facio-digito-genital syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 725434009 | Autosomal recessive facio-digito-genital syndrome | Non-standard |
Synonyms
Alternative names recorded for Autosomal recessive facio-digito-genital syndrome across source vocabularies.
- Aarskog-like syndrome
- Autosomal recessive faciodigitogenital syndrome
- Autosomal recessive faciodigitogenital syndrome (disorder)
- Facio-digito-genital syndrome Kuwait type
- síndrome faciodigitogenital autosómico recesivo
- síndrome faciodigitogenital autosómico recesivo (trastorno)
- Teebi Naguib Alawadi syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(40)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of digit
- 1Developmental hereditary disorder
- 1Genitourinary congenital anomalies
- 1Hereditary disorder by system
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of limb
- 2Congenital anomaly of lower trunk
- 2Developmental disorder
- 2Disorder of body system
- 2Disorder of digit
- 2Disorder of the genitourinary system
- 2Hereditary disease
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with limb defect as major feature
- 3Congenital abnormality of lower limb and pelvic girdle
- 3Congenital anomaly of face
- 3Congenital anomaly of trunk
- 3Congenital malformation
- 3Disease
- 3Disorder of abdominopelvic segment of trunk
- 3Disorder of limb
- 3Genetic disease
- 3Multiple system malformation syndrome
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