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715464002: Microcephalus microcornea syndrome of Seemanova type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302716010 Microcephalus microcornea syndrome of Seemanova type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302717018 Microcephalus microcornea syndrome of Seemanova type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302718011 Microcephaly microcornea syndrome Seemanova type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302719015 Seemanova Lesny syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400909014 Microcephaly-microcornea syndrome, Seemanova type is characterized by microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity. It has been described in two patients (a male and his sister's son). Both patients also presented with facial dysmorphism, including upslanting palpebral fissures, epicanthal folds, highly arched palate, microstomia, and retrognathia. This syndrome is transmitted as an X-linked trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400910016 Microcephaly-microcornea syndrome, Seemanova type is characterised by microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity. It has been described in two patients (a male and his sister's son). Both patients also presented with facial dysmorphism, including upslanting palpebral fissures, epicanthal folds, highly arched palate, microstomia, and retrognathia. This syndrome is transmitted as an X-linked trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302716010 Microcephalus microcornea syndrome of Seemanova type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302717018 Microcephalus microcornea syndrome of Seemanova type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302718011 Microcephaly microcornea syndrome Seemanova type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3302719015 Seemanova Lesny syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302720014 Extremely rare syndrome with features of microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity. This syndrome is transmitted as an X-linked trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400909014 Microcephaly-microcornea syndrome, Seemanova type is characterized by microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity. It has been described in two patients (a male and his sister's son). Both patients also presented with facial dysmorphism, including upslanting palpebral fissures, epicanthal folds, highly arched palate, microstomia, and retrognathia. This syndrome is transmitted as an X-linked trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400910016 Microcephaly-microcornea syndrome, Seemanova type is characterised by microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity. It has been described in two patients (a male and his sister's son). Both patients also presented with facial dysmorphism, including upslanting palpebral fissures, epicanthal folds, highly arched palate, microstomia, and retrognathia. This syndrome is transmitted as an X-linked trait. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
521851000274114 Seemanova-Lesny-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3392031001000111 Mikrozephalie-Mikrokornea-Syndrom, Typ Seemanova de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929391000172110 syndrome de Seemanova-Lesny fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1001201000172114 microcéphalie-microcornée type Seemanova fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929391000172110 syndrome de Seemanova-Lesny fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1001201000172114 microcéphalie-microcornée type Seemanova fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
521851000274114 Seemanova-Lesny-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3392031001000111 Mikrozephalie-Mikrokornea-Syndrom, Typ Seemanova 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
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a microcéphalie false Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a Microcornea true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus microcornea syndrome of Seemanova type (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus microcornea syndrome of Seemanova type (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalus microcornea syndrome of Seemanova type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalus microcornea syndrome of Seemanova type (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalus microcornea syndrome of Seemanova type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus microcornea syndrome of Seemanova type (disorder) Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus microcornea syndrome of Seemanova type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus microcornea syndrome of Seemanova type (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus microcornea syndrome of Seemanova type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus microcornea syndrome of Seemanova type (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Interprets Birth head circumference true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus microcornea syndrome of Seemanova type (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Is a Congenital microcephaly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus microcornea syndrome of Seemanova type (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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