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783555001: Hypotrichosis and deafness syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3759333015 Hypotrichosis and deafness syndrome en Synonym Active Case insensitive SNOMED CT core
3759334014 Hypotrichosis and deafness syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3759335010 A syndromic genetic deafness with characteristics of erythrokeratoderma, hypotrichosis, nail dystrophy and sensorineural hearing loss. Erythema, recurrent skin infections and mucositis have also been associated. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypotrichosis and deafness syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hypotrichosis and deafness syndrome Is a Hypotrichosis true Inferred relationship Some
Hypotrichosis and deafness syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Some 1
Hypotrichosis and deafness syndrome Is a Developmental and/or congenital abnormality of nail false Inferred relationship Some
Hypotrichosis and deafness syndrome Finding site Nail unit structure true Inferred relationship Some 1
Hypotrichosis and deafness syndrome Is a Erythrokeratoderma true Inferred relationship Some
Hypotrichosis and deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Some
Hypotrichosis and deafness syndrome Is a Sensorineural hearing loss true Inferred relationship Some
Hypotrichosis and deafness syndrome Is a Keratosis false Inferred relationship Some
Hypotrichosis and deafness syndrome Is a Genetic disorder of nail true Inferred relationship Some
Hypotrichosis and deafness syndrome Finding site Hair structure true Inferred relationship Some 2
Hypotrichosis and deafness syndrome Finding site Structure of auditory system true Inferred relationship Some 4
Hypotrichosis and deafness syndrome Interprets Keratinisation true Inferred relationship Some 3
Hypotrichosis and deafness syndrome Has interpretation Abnormal true Inferred relationship Some 3
Hypotrichosis and deafness syndrome Interprets Hearing true Inferred relationship Some 5
Hypotrichosis and deafness syndrome Associated morphology Growth alteration true Inferred relationship Some 2
Hypotrichosis and deafness syndrome Is a Dystrophia unguium true Inferred relationship Some
Hypotrichosis and deafness syndrome Associated morphology Dystrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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