FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

717945001: Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3324423016 Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324424010 BRESEK syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3324426012 X-linked mental retardation Reish type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5155338014 Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5155339018 Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5155341017 BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5155340016 X-linked syndrome with characteristics of brain anomalies, severe intellectual disability, ectodermal dysplasia, skeletal deformities (vertebral anomalies, scoliosis, polydactyly), ear/eye anomalies (maldevelopment, small optic nerves, low set and large ears with hearing loss) and kidney dysplasia/hypoplasia (giving the acronym BRESEK syndrome). It has been described in two brothers, one of who died shortly after birth. One of the brothers also had Hirschsprung disease and Cleft palate/cryptorchidism (giving the acronym: BRESHECK syndrome). Transmission is X-linked dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
BRESEK syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
BRESEK syndrome Is a Mental retardation false Inferred relationship Some
BRESEK syndrome Is a X-linked hereditary disease false Inferred relationship Some
BRESEK syndrome Associated morphology Developmental anomaly false Inferred relationship Some 1
BRESEK syndrome Occurrence Congenital true Inferred relationship Some 1
BRESEK syndrome Is a Intellectual disability true Inferred relationship Some
BRESEK syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
BRESEK syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
BRESEK syndrome Is a Developmental hereditary disorder true Inferred relationship Some
BRESEK syndrome Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Some
BRESEK syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 2
BRESEK syndrome Has interpretation Impaired true Inferred relationship Some 2
BRESEK syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 3
BRESEK syndrome Has interpretation Impaired true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start