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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
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
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculoauricular syndrome Schorderet type Is a Congenital anomaly of eye true Inferred relationship Some
Oculoauricular syndrome Schorderet type Is a Multiple system malformation syndrome true Inferred relationship Some
Oculoauricular syndrome Schorderet type Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Oculoauricular syndrome Schorderet type Is a Congenital abnormality of external ear true Inferred relationship Some
Oculoauricular syndrome Schorderet type Is a Auditory system hereditary disorder true Inferred relationship Some
Oculoauricular syndrome Schorderet type Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Oculoauricular syndrome Schorderet type Associated morphology anomalie du développement false Inferred relationship Some 2
Oculoauricular syndrome Schorderet type Occurrence Congenital true Inferred relationship Some 2
Oculoauricular syndrome Schorderet type Finding site Eye structure true Inferred relationship Some 2
Oculoauricular syndrome Schorderet type Associated morphology anomalie du développement false Inferred relationship Some 1
Oculoauricular syndrome Schorderet type Occurrence Congenital true Inferred relationship Some 1
Oculoauricular syndrome Schorderet type Finding site External ear structure true Inferred relationship Some 1
Oculoauricular syndrome Schorderet type Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculoauricular syndrome Schorderet type Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculoauricular syndrome Schorderet type Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Oculoauricular syndrome Schorderet type Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Oculoauricular syndrome Schorderet type Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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