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699300009: Oculofaciocardiodental syndrome (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
2983577012 Microphthalmia, cataract, radiculomegaly and septal heart defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983599016 Oculo-facio-cardio-dental syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983608013 Microphthalmia syndromic 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983632018 Oculofaciocardiodental syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983690011 Oculofaciocardiodental syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983577012 Microphthalmia, cataract, radiculomegaly and septal heart defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983577012 Microphthalmia, cataract, radiculomegaly and septal heart defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983599016 Oculo-facio-cardio-dental syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983599016 Oculo-facio-cardio-dental syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983608013 Microphthalmia syndromic 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983608013 Microphthalmia syndromic 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983632018 Oculofaciocardiodental syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983632018 Oculofaciocardiodental syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2983690011 Oculofaciocardiodental syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2983690011 Oculofaciocardiodental syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3453581001000111 Okulo-fazio-kardio-dentales Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873321000172115 syndrome OFCD (oculo-facio-cardio-dentaire) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1019091000172111 syndrome oculo-facio-cardio-dentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873321000172115 syndrome OFCD (oculo-facio-cardio-dentaire) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1019091000172111 syndrome oculo-facio-cardio-dentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3453581001000111 Okulo-fazio-kardio-dentales Syndrom 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
Oculofaciocardiodental syndrome (disorder) Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Oculofaciocardiodental syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Oculofaciocardiodental syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Oculofaciocardiodental syndrome (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Oculofaciocardiodental syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculofaciocardiodental syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculofaciocardiodental syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculofaciocardiodental syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oculofaciocardiodental syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oculofaciocardiodental syndrome (disorder) Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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