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86166000: Alopecia universalis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
142888018 Alopecia universalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
828372016 Alopecia universalis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235101014 Universal alopecia areata en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
142888018 Alopecia universalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
142888018 Alopecia universalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
828372016 Alopecia universalis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
828372016 Alopecia universalis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235101014 Universal alopecia areata en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1235101014 Universal alopecia areata en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3450871001000118 Alopecia universalis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1014341000172119 pelade universelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1014341000172119 pelade universelle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3450871001000118 Alopecia universalis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Alopecia universalis (disorder) Is a Alopecia areata true Inferred relationship Existential restriction modifier (core metadata concept)
Alopecia universalis (disorder) Finding site Hair structure false Inferred relationship Existential restriction modifier (core metadata concept)
Alopecia universalis (disorder) Finding site Hair structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Alopecia universalis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Alopecia universalis (disorder) Associated morphology Absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Alopecia universalis (disorder) Finding site Hair structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Alopecia universalis (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Alopecia universalis (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare genetic syndromic intellectual disability that is characterized by congenital permanent alopecia universalis, intellectual disability, psychomotor epilepsy and periodontitis (pyorrhea). Total permanent alopecia and pyorrhea are invariably concomitant while intellectual disability and psychomotor epilepsy are observed in most patients. No other abnormality of nails or skin (apart from absence of hair) has been reported. Transmission is autosomal dominant. Is a True Alopecia universalis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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