OMOP Concept 4028387
Disorder of integument
StandardConditionSNOMED128598002Disorder
Maps from
18
Descendants
10,860
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
18 source codes normalize to Disorder of integument via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Disorder of integument across source vocabularies.
- Disorder of integument (disorder)
- trastorno del tegumento
- trastorno tegumentario
- trastorno tegumentario (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(10,860)Included automatically when you query with descendants.
- 1Dermatological complication of procedure
- 1Disorder involving the integument of fetus OR newborn
- 1Disorder of keratinization
- 1Disorder of skin and/or subcutaneous tissue
- 1Disseminated dermatophytosis
- 1Habit tic
- 1Hamartoma of integument
- 1Hereditary disorder of the integument
- 1Injury of integument
- 1Loss of integument's waterproofing
- 1Neoplasm of integumentary system
- 1Superficial mycosis
- 1Vogt-Koyanagi-Harada disease
- 2Abrasion of female genital organ
- 2Abrasion of scalp
- 2Abrasion of scrotum
- 2Abscess of skin and/or subcutaneous tissue
- 2Absence of fingerprints with congenital milia syndrome
- 2Acanthosis nigricans
- 2Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome
- 2Ackerman syndrome
- 2Acquired disorder of keratinization
- 2Acroosteolysis, keloid-like lesions, premature aging syndrome
- 2Acute radiodermatitis due to and following radiotherapy
- 2Adams-Oliver syndrome
- 2ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome
- 2Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 2AGel amyloidosis
- 2AKT2-related familial partial lipodystrophy
- 2Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
- 2Alopecia, contracture, dwarfism, intellectual disability syndrome
- 2Alopecia, epilepsy, intellectual disability syndrome Moynahan type
- 2Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
- 2Alopecia, progressive neurological defect, endocrinopathy syndrome
- 2Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome
- 2Amaurosis hypertrichosis syndrome
- 2Amelo-onycho-hypohidrotic syndrome
- 2Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome
- 2Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation
- 2Anonychia with microcephaly syndrome
- 2Aplasia cutis congenita with epibulbar dermoid syndrome
- 2Aplasia cutis congenita with intestinal lymphangiectasia syndrome
- 2Aplasia cutis with myopia syndrome
- 2Artefactual skin disease
- 2Arthrogryposis and ectodermal dysplasia syndrome
- 2Autosomal dominant familial wooly hair
- 2Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
- 2Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
- 2Autosomal recessive cutis laxa type 2A
- 2Autosomal recessive familial wooly hair
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