OMOP Concept 134757
Ectodermal dysplasia
StandardConditionSNOMED8654005Disorder
Maps from
13
Descendants
158
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
13 source codes normalize to Ectodermal dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141533 | Ectodermal dysplasia | Non-standard |
| CIM10 | Q82.4 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| HPO | HP_0000968 | Ectodermal dysplasia | Non-standard |
| ICD10 | Q82.4 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| ICD10CM | Q82.4 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| ICD10CN | Q82.4 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| ICD10CN | Q82.400 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| ICD10GM | Q82.4 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| ICD9CM | 757.31 | Congenital ectodermal dysplasia | Non-standard |
| KCD7 | Q82.4 | Ectodermal dysplasia (anhidrotic) | Non-standard |
| MeSH | D004476 | Ectodermal Dysplasia | Non-standard |
| Nebraska Lexicon | 8654005 | Ectodermal dysplasia | Non-standard |
| Read | PH30.00 | Congenital ectodermal dysplasia | Non-standard |
Synonyms
Alternative names recorded for Ectodermal dysplasia across source vocabularies.
- displasia ectodérmica
- displasia ectodérmica (trastorno)
- Ectodermal dysplasia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Congenital ectodermal defect
- 1Genodermatosis
- 2Congenital anomaly of skin
- 2Congenital malformation
- 2Disorder of embryonic structure
- 3Congenital anomaly of integument
- 3Congenital disease
- 3Developmental disorder
- 3Disease
- 3Disorder of skin
- 4Clinical finding
- 4Disorder involving the integument of fetus OR newborn
- 4Disorder of fetus and/or newborn
- 4Disorder of skin and/or subcutaneous tissue
- 4Skin finding
- 5Disorder of integument
- 5Disorder of soft tissue
- 5General finding of soft tissue
- 5Integumentary system finding
- 5Skin AND/OR mucosa finding
- 6Disorder of body system
Narrower concepts
(158)Included automatically when you query with descendants.
- 1Ackerman syndrome
- 1Alopecia, contracture, dwarfism, intellectual disability syndrome
- 1Amelo-onycho-hypohidrotic syndrome
- 1Autosomal recessive popliteal pterygium syndrome
- 1Barber-Say syndrome
- 1Blepharocheilodontic syndrome
- 1Cerebellar ataxia and ectodermal dysplasia
- 1Choroidal atrophy and alopecia syndrome
- 1Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome
- 1Dyskeratosis congenita
- 1Ectodermal dysplasia and sensorineural deafness syndrome
- 1Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome
- 1Ectodermal dysplasia-ocular malformation syndrome
- 1Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome
- 1Ectodermal dysplasia with hair-tooth defects
- 1Ectodermal dysplasia with nail defect
- 1Ectodermal dysplasia with natal teeth Turnpenny type
- 1Ectodermal dysplasia with sweating defect
- 1Focal facial dermal dysplasia
- 1Hypertrichosis cubiti
- 1Hypotrichosis with juvenile macular degeneration syndrome
- 1Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome
- 1Johnson neuroectodermal syndrome
- 1KID syndrome
- 1Kirman syndrome
- 1Lelis syndrome
- 1Limb mammary syndrome
- 1Lymphedema hypoparathyroidism syndrome
- 1Odonto-tricho-ungual-digito-palmar syndrome
- 1Oliver McFarlane syndrome
- 1Oral-facial-digital syndrome
- 1Papillon-Lefèvre syndrome
- 1Scalp, ear, nipple syndrome
- 1Skin fragility, wooly hair, palmoplantar keratoderma syndrome
- 1Trichodysplasia with amelogenesis imperfecta syndrome
- 1Trichothiodystrophy
- 1Zlotogora Ogur syndrome
- 2Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
- 2Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome
- 2Autosomal dominant dyskeratosis congenita
- 2Autosomal recessive dyskeratosis congenita
- 2Autosomal recessive keratitis-ichthyosis-deafness syndrome
- 2Berlin syndrome
- 2BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome
- 2Clastothrix
- 2Conductive deafness, ptosis, skeletal anomalies syndrome
- 2Contracture with ectodermal dysplasia and orofacial cleft syndrome
- 2Cranioectodermal dysplasia
- 2Deafness with onychodystrophy syndrome
- 2Ectodermal dysplasia syndactyly syndrome
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