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699297004: Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2983700013 Ohdo syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2983702017 Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983727012 X-linked Ohdo syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643148017 Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643149013 Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983555013 Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983700013 Ohdo syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983700013 Ohdo syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2983702017 Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983702017 Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2983702017 Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983727012 X-linked Ohdo syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983727012 X-linked Ohdo syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643148017 Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643148017 Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643149013 Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643149013 Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
599831000274113 BMRS vom Typ Maat-Kievit-Brunner de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3417821001000111 Blepharophimose-Intelligenzminderung-Syndrom Typ MKB de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5805431000241113 BMRS (blepharophimosis and mental retardation syndrome) de type Maat-Kievit-Brunner fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5805441000241115 syndrome de blépharophimosis et déficience intellectuelle de type Maat-Kievit-Brunner fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5805431000241113 BMRS (blepharophimosis and mental retardation syndrome) de type Maat-Kievit-Brunner fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5805441000241115 syndrome de blépharophimosis et déficience intellectuelle de type Maat-Kievit-Brunner fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
599831000274113 BMRS vom Typ Maat-Kievit-Brunner de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3417821001000111 Blepharophimose-Intelligenzminderung-Syndrom Typ MKB de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ohdo syndrome, Maat-Kievit-Brunner type Is a Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth false Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Tooth structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 6
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 6
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology Narrowed structure (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 5
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Structure of palpebral fissure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 7
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Eyelid structure false Inferred relationship Existential restriction modifier (core metadata concept) 7
Ohdo syndrome, Maat-Kievit-Brunner type Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Eyelid structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Heart structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Eyelid structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ohdo syndrome, Maat-Kievit-Brunner type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology Narrowed structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ohdo syndrome, Maat-Kievit-Brunner type Finding site Structure of palpebral fissure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ohdo syndrome, Maat-Kievit-Brunner type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ohdo syndrome, Maat-Kievit-Brunner type Associated morphology Deformity (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ohdo syndrome, Maat-Kievit-Brunner type Is a Blepharophimosis, intellectual disability syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Ohdo syndrome, Maat-Kievit-Brunner type Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ohdo syndrome, Maat-Kievit-Brunner type Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 4
Ohdo syndrome, Maat-Kievit-Brunner type Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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