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763815000: Oculoauricular syndrome Schorderet 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
3644087014 Oculoauricular syndrome Schorderet type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3644088016 Oculoauricular syndrome Schorderet type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5404220012 Oculoauricular syndrome, Schorderet type is a rare, genetic developmental defect during embryogenesis syndrome characterized by various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy) and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisures, abnormal bridge connecting the crus of the helix and the antihelix, narrow external acoustic meatus, and lobule aplasia). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404221011 Oculoauricular syndrome, Schorderet type is a rare, genetic developmental defect during embryogenesis syndrome characterised by various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy) and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisures, abnormal bridge connecting the crus of the helix and the antihelix, narrow external acoustic meatus, and lobule aplasia). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3644087014 Oculoauricular syndrome Schorderet type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3644088016 Oculoauricular syndrome Schorderet type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3644093018 A rare genetic developmental defect during embryogenesis with characteristics of various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy) and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisure, abnormal bridge connecting the crus of the helix and the anthelix, narrow external acoustic meatus and lobule aplasia). There is evidence the disease is caused by homozygous mutation in the HMX1 gene on chromosome 4p16. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404220012 Oculoauricular syndrome, Schorderet type is a rare, genetic developmental defect during embryogenesis syndrome characterized by various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy) and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisures, abnormal bridge connecting the crus of the helix and the antihelix, narrow external acoustic meatus, and lobule aplasia). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404221011 Oculoauricular syndrome, Schorderet type is a rare, genetic developmental defect during embryogenesis syndrome characterised by various ophthalmic anomalies (including congenital microphthalmia, microcornea, cataract, anterior segment dysgenesis, ocular coloboma and early onset rod-cone dystrophy) and abnormal external ears (low-set pinna with crumpled helix, narrow intertragic incisures, abnormal bridge connecting the crus of the helix and the antihelix, narrow external acoustic meatus, and lobule aplasia). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
542631000274113 Okuloaurikuläres Syndrom, Typ Schorderet de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3426861001000114 Okuloaurikuläres Syndrom Typ Schorderet de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1019401000172111 syndrome oculo-auriculaire type Schorderet fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1019401000172111 syndrome oculo-auriculaire type Schorderet fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
542631000274113 Okuloaurikuläres Syndrom, Typ Schorderet de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3426861001000114 Okuloaurikuläres Syndrom Typ Schorderet 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
Oculoauricular syndrome Schorderet type (disorder) Is a Congenital anomaly of eye true Inferred relationship Existential restriction modifier (core metadata concept)
Oculoauricular syndrome Schorderet type (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Oculoauricular syndrome Schorderet type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oculoauricular syndrome Schorderet type (disorder) Is a Congenital abnormality of external ear true Inferred relationship Existential restriction modifier (core metadata concept)
Oculoauricular syndrome Schorderet type (disorder) Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oculoauricular syndrome Schorderet type (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oculoauricular syndrome Schorderet type (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculoauricular syndrome Schorderet type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculoauricular syndrome Schorderet type (disorder) Finding site Eye structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculoauricular syndrome Schorderet type (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculoauricular syndrome Schorderet type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculoauricular syndrome Schorderet type (disorder) Finding site External ear structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculoauricular syndrome Schorderet type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculoauricular syndrome Schorderet type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculoauricular syndrome Schorderet type (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculoauricular syndrome Schorderet type (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculoauricular syndrome Schorderet type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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