OMOP Concept 37116665
Camptodactyly taurinuria syndrome
StandardConditionSNOMED733466005Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Camptodactyly taurinuria syndrome across source vocabularies.
- Camptodactyly taurinuria syndrome (disorder)
- Familial streblodactyly with amino-aciduria
- síndrome de camptodactilia con taurinuria
- síndrome de camptodactilia con taurinuria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(69)Roll up to these when you need a wider cohort.
- 1Camptodactyly of finger
- 1Hereditary camptodactyly
- 1Inherited aminoaciduria
- 1Multiple malformation syndrome with limb defect as major feature
- 2Aminoaciduria
- 2Autosomal dominant hereditary disorder
- 2Camptodactyly
- 2Congenital anomaly of finger
- 2Congenital deformity of hand
- 2Developmental hereditary disorder
- 2Finding of musculoskeletal structure of finger
- 2Flexion deformity of hand
- 2Hereditary disorder of musculoskeletal system
- 2Hereditary metabolic disease
- 2Multiple system malformation syndrome
- 3Aciduria
- 3Amino acid above reference range
- 3Autosomal hereditary disorder
- 3Congenital abnormal shape of digit
- 3Congenital anomaly of digit
- 3Congenital anomaly of hand
- 3Congenital deformity of musculoskeletal system
- 3Congenital deformity of upper limb
- 3Congenital malformation syndrome
- 3Deformity of hand
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