FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

717944002: Branchiogenic deafness syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3324418016 Branchiogenic deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324419012 Branchiogenic deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3324420018 Megarbane Loiselet syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Branchiogenic deafness syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Branchiogenic deafness syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Branchiogenic deafness syndrome Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier
Branchiogenic deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Branchiogenic deafness syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 2
Branchiogenic deafness syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Branchiogenic deafness syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Branchiogenic deafness syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Branchiogenic deafness syndrome Finding site Ear structure false Inferred relationship Existential restriction modifier 3
Branchiogenic deafness syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 1
Branchiogenic deafness syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Branchiogenic deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Branchiogenic deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Branchiogenic deafness syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start