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764861005: Intellectual disability Birk-Barel type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3655431013 Intellectual disability, hypotonia, facial dysmorphism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655432018 Intellectual disability Birk-Barel type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655433011 Intellectual disability Birk-Barel type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655434017 Birk Barel mental retardation dysmorphism syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3655435016 KCNK9 (potassium two pore domain channel subfamily K member 9) imprinting syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404402018 Intellectual disability, Birk-Barel type is a rare, genetic, syndromic intellectual disability characterized by congenital central hypotonia, developmental delay, moderate to severe intellectual disability and subtle dysmorphic features which evolve over time (dolichocephaly, myopathic facies, ptosis, short and broad philtrum, tented upper lip vermillion, palatal anomalies, mild micro- and/or retrognathia). Patients present reduced facial movements, lethargy, weak cry, transient neonatal hypoglycemia, severe feeding difficulties and failure to thrive. Dysphagia, particularly of solid food, asthenic body build, joint contractures and scoliosis are additional features. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404403011 Intellectual disability, Birk-Barel type is a rare, genetic, syndromic intellectual disability characterised by congenital central hypotonia, developmental delay, moderate to severe intellectual disability and subtle dysmorphic features which evolve over time (dolichocephaly, myopathic facies, ptosis, short and broad philtrum, tented upper lip vermillion, palatal anomalies, mild micro- and/or retrognathia). Patients present reduced facial movements, lethargy, weak cry, transient neonatal hypoglycaemia, severe feeding difficulties and failure to thrive. Dysphagia, particularly of solid food, asthenic body build, joint contractures and scoliosis are additional features. 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
Intellectual disability Birk-Barel type Is a Multiple system malformation syndrome true Inferred relationship Some
Intellectual disability Birk-Barel type Is a Intellectual disability true Inferred relationship Some
Intellectual disability Birk-Barel type Associated morphology Developmental anomaly false Inferred relationship Some 1
Intellectual disability Birk-Barel type Occurrence Congenital true Inferred relationship Some 1
Intellectual disability Birk-Barel type Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Intellectual disability Birk-Barel type Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Intellectual disability Birk-Barel type Interprets Intellectual ability (observable entity) true Inferred relationship Some 2
Intellectual disability Birk-Barel type Has interpretation Impaired true Inferred relationship Some 2
Intellectual disability Birk-Barel type Interprets Adaptation behavior (observable entity) true Inferred relationship Some 3
Intellectual disability Birk-Barel type Has interpretation Impaired true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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