Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
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Source codes that map to this concept
2 source codes normalize to Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565604 | Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia | Non-standard |
| Nebraska Lexicon | 239050000 | Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections | Non-standard |
Synonyms
Alternative names recorded for Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections across source vocabularies.
- Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections (disorder)
- ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome
- ANOTHER syndrome
- Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome
- síndrome de alopecia, distrofia ungueal, complicaciones oftálmicas, disfunción tiroidea, hipohidrosis, efélides, enteropatía e infecciones respiratorias
- síndrome de alopecia, distrofia ungueal, complicaciones oftálmicas, disfunción tiroidea, hipohidrosis, efélides, enteropatía e infecciones respiratorias (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(32)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Ectodermal dysplasia with sweating defect
- 1Hereditary disorder of the integument
- 2Autosomal hereditary disorder
- 2Developmental disorder
- 2Disorder of integument
- 2Ectodermal dysplasia
- 2Finding of sweating
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital ectodermal defect
- 3Disease
- 3Disorder of body system
- 3Functional finding
- 3Genetic disease
- 3Genodermatosis
- 3Integumentary system finding
- 3Skin finding
- 4Clinical finding
- 4Congenital anomaly of skin
- 4Congenital malformation
- 4Disorder of embryonic structure
- 4General finding of soft tissue
- 4Skin AND/OR mucosa finding
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