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725100001: Craniolenticulosutural dysplasia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3438536016 Craniolenticulosutural dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438537013 Craniolenticulosutural dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438538015 Boyadjiev Jabs syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403397013 Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403398015 Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterised by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalised skeletal dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3438536016 Craniolenticulosutural dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438537013 Craniolenticulosutural dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438538015 Boyadjiev Jabs syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3438539011 Syndrome that is characterized by the specific association of large and late-closing fontanelles, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia. Patients have abnormal hair, frontal bossing, hyperpigmentation with capillary hemangioma of the forehead, macrocephaly, significant hypertelorism, and a broad and prominent nose. In addition patients have Y-shaped sutural cataracts. All affected individuals have proportionate short stature but intellectual development is normal. The syndrome maps to chromosome 14q13-q21 and causative mutations have been identified in the SEC23A gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3438540013 Syndrome that is characterised by the specific association of large and late-closing fontanelles, hypertelorism, early-onset cataract and mild generalised skeletal dysplasia. Patients have abnormal hair, frontal bossing, hyperpigmentation with capillary haemangioma of the forehead, macrocephaly, significant hypertelorism, and a broad and prominent nose. In addition patients have Y-shaped sutural cataracts. All affected individuals have proportionate short stature but intellectual development is normal. The syndrome maps to chromosome 14q13-q21 and causative mutations have been identified in the SEC23A gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403397013 Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403398015 Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterised by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalised skeletal dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3429281001000111 Dysplasie, kranio-lentikulo-suturale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
895331000172110 dysplasie cranio-lenticulo-suturale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
937361000172112 syndrome de Boyadjiev-Jabs fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
895331000172110 dysplasie cranio-lenticulo-suturale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
937361000172112 syndrome de Boyadjiev-Jabs fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429281001000111 Dysplasie, kranio-lentikulo-suturale 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
Craniolenticulosutural dysplasia (disorder) Is a Hypertelorism true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Late fontanel closure false Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Congenital enlargement of fontanel true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Skeletal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Short stature disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Interprets Fontanel closure false Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniolenticulosutural dysplasia (disorder) Associated morphology Congenital enlargement false Inferred relationship Existential restriction modifier (core metadata concept) 5
Craniolenticulosutural dysplasia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Craniolenticulosutural dysplasia (disorder) Finding site Entire fontanel of skull (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 5
Craniolenticulosutural dysplasia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 6
Craniolenticulosutural dysplasia (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniolenticulosutural dysplasia (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniolenticulosutural dysplasia (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 6
Craniolenticulosutural dysplasia (disorder) Finding site Sphenoid bone structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 6
Craniolenticulosutural dysplasia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniolenticulosutural dysplasia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniolenticulosutural dysplasia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniolenticulosutural dysplasia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniolenticulosutural dysplasia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniolenticulosutural dysplasia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniolenticulosutural dysplasia (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniolenticulosutural dysplasia (disorder) Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniolenticulosutural dysplasia (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniolenticulosutural dysplasia (disorder) Finding site Sphenoid bone structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniolenticulosutural dysplasia (disorder) Finding site Entire fontanel of skull (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniolenticulosutural dysplasia (disorder) Associated morphology Congenital enlargement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniolenticulosutural dysplasia (disorder) Is a Defect of skull ossification (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Interprets Bone formation false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniolenticulosutural dysplasia (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniolenticulosutural dysplasia (disorder) Is a Functional finding false Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniolenticulosutural dysplasia (disorder) Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniolenticulosutural dysplasia (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Craniolenticulosutural dysplasia (disorder) Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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