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720567008: Bosley Salih Alorainy syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3321265014 Bosley Salih Alorainy syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3321266010 Bosley Salih Alorainy syndrome en Synonym Active Case sensitive SNOMED CT core
3321267018 Syndrome with characteristics of variable horizontal gaze dysfunction, profound and bilateral sensorineural deafness associated commonly with severe inner ear maldevelopment, cerebrovascular anomalies, cardiac malformation, developmental delay and occasionally autism. The syndrome is caused by homozygous mutations in the HOXA1 gene (7p15.2) and is transmitted in an autosomal recessive manner. The syndrome overlaps clinically and genetically with Athabaskan brain dysfunction syndrome, however unlike Athabaskan brain dysfunction syndrome it does not manifest central hypoventilation. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bosley Salih Alorainy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Bosley Salih Alorainy syndrome Finding site Structure of heart true Inferred relationship Some 1
Bosley Salih Alorainy syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Bosley Salih Alorainy syndrome Occurrence Congenital true Inferred relationship Some 1
Bosley Salih Alorainy syndrome Is a Congenital hearing disorder false Inferred relationship Some
Bosley Salih Alorainy syndrome Finding site Structure of auditory system true Inferred relationship Some 2
Bosley Salih Alorainy syndrome Interprets Hearing true Inferred relationship Some 3
Bosley Salih Alorainy syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Bosley Salih Alorainy syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Some
Bosley Salih Alorainy syndrome Has interpretation Impaired true Inferred relationship Some 3
Bosley Salih Alorainy syndrome Is a Congenital heart disease true Inferred relationship Some
Bosley Salih Alorainy syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
Bosley Salih Alorainy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Bosley Salih Alorainy syndrome Is a Hearing loss associated with syndrome true Inferred relationship Some
Bosley Salih Alorainy syndrome Is a Auditory system hereditary disorder true Inferred relationship Some
Bosley Salih Alorainy syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Bosley Salih Alorainy syndrome Finding site Ear structure false Inferred relationship Some 2
Bosley Salih Alorainy syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Bosley Salih Alorainy syndrome Occurrence Congenital true Inferred relationship Some 2
Bosley Salih Alorainy syndrome Finding site Structure of heart false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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