OMOP Concept 443401
Congenital connective tissue disorder
StandardConditionSNOMED363039000Disorder
Maps from
3
Descendants
201
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Congenital connective tissue disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 155724 | Congenital trigger thumb | Non-standard |
| Nebraska Lexicon | 363039000 | Congenital connective tissue disorder | Non-standard |
| Read | PGz4.00 | Unspecified anomaly of connective tissue | Non-standard |
Synonyms
Alternative names recorded for Congenital connective tissue disorder across source vocabularies.
- Congenital connective tissue disorder (disorder)
- trastorno congénito del tejido conectivo
- trastorno congénito del tejido conjuntivo
- trastorno congénito del tejido conjuntivo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(201)Included automatically when you query with descendants.
- 116q24.1 microdeletion syndrome
- 1Allantoic cyst
- 1Aneurysm osteoarthritis syndrome
- 1Banki syndrome
- 1Bilateral developmental anomaly of pleurae
- 1Congenital absence of tendon
- 1Congenital anomaly of cartilage
- 1Congenital anomaly of peritoneum
- 1Congenital anomaly of pleural folds
- 1Congenital deformity of mitral valve annulus
- 1Congenital epicardial cyst
- 1Congenital Fanconi syndrome
- 1Congenital generalized lipodystrophy
- 1Congenital hypoplasia of annulus fibrosus of aorta
- 1Congenital macular corneal dystrophy
- 1Congenital malformation of vitreous humor
- 1Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
- 1Congenital rectovaginal constriction of Jersey cattle
- 1Congenital short costocoracoid ligament
- 1Congenital shortening of tendon
- 1Congenital stromal corneal dystrophy
- 1Congenital syphilitic osteochondritis
- 1Congenital trigger finger
- 1Cutaneous asthenia in dogs AND/OR cats
- 1Dilatation of tricuspid annulus
- 1Ehlers-Danlos and osteogenesis imperfecta syndrome
- 1Ehlers-Danlos syndrome
- 1Extensor tendons of finger anomalies
- 1Familial articular hypermobility syndrome
- 1Farber's lipogranulomatosis
- 1Hereditary equine regional dermal asthenia
- 1Hypoplasia of left atrioventricular valve annulus in double inlet ventricle
- 1Hypoplasia of mitral valve annulus
- 1Hypoplasia of right atrioventricular valve annulus in double inlet ventricle
- 1Inherited cutis laxa
- 1Late congenital syphilitic osteochondropathy
- 1Leydig cell agenesis
- 1Mandibuloacral dysostosis
- 1Marfanoid habitus, inguinal hernia, advanced bone age syndrome
- 1Neonatal Marfan syndrome
- 1Progeroid and marfanoid aspect, lipodystrophy syndrome
- 1Pulmonary valve ring hypoplasia
- 1Schistosomus reflexus
- 1Severe myopia, generalized joint laxity, short stature syndrome
- 1Tricuspid annulus hypoplasia
- 1Williams syndrome
- 2Agenesis of nasal cartilages
- 2Arthrochalasia Ehlers-Danlos syndrome
- 2Brittle cornea syndrome
- 2Classical-like Ehlers-Danlos syndrome type 1
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