OMOP Concept 201958
Fetal and/or neonatal disorder of integument
StandardConditionSNOMED111474003Disorder
Maps from
18
Descendants
927
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 Fetal and/or neonatal disorder of integument via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Fetal and/or neonatal disorder of integument across source vocabularies.
- Fetal and/or neonatal disorder of integument (disorder)
- trastorno fetal y/o neonatal de sistema tegumentario
- trastorno fetal y/o neonatal de sistema tegumentario (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(927)Included automatically when you query with descendants.
- 1Acroosteolysis, keloid-like lesions, premature aging syndrome
- 1Autosomal recessive cutis laxa type 2A
- 1Congenital accessory skin tag
- 1Congenital anomaly of integument
- 1Congenital benign giant pigmented nevus of skin
- 1Congenital cutaneous angiomatosis
- 1Congenital cutaneous mastocytosis
- 1Congenital dermal melanocytosis
- 1Congenital diffuse lipomatosis
- 1Congenital generalized lipodystrophy
- 1Congenital hamartoma of skin
- 1Congenital keratoderma
- 1Congenital lethal erythroderma
- 1Congenital syphilitic pemphigus
- 1Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
- 1Cutis marmorata telangiectasia congenita
- 1Cutis tricolor
- 1de Barsey syndrome
- 1Diffuse fetal skin edema
- 1Encephalocraniocutaneous lipomatosis
- 1Erythema palmare hereditarium
- 1Extensive congenital erosions, vesicles and reticulate scarring
- 1Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome
- 1Facial dysmorphism, immunodeficiency, livedo, short stature syndrome
- 1Farber's lipogranulomatosis
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