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429753001: Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2008. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2688300012 Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2694575011 Congenital nonprogressive myopathy with Moebius and Robin sequences en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2695275018 Carey Fineman Ziter syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2688300012 Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2694575011 Congenital nonprogressive myopathy with Moebius and Robin sequences en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2695275018 Carey Fineman Ziter syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3383211001000115 Carey-Fineman-Ziter-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5834731000241111 myopathie congénitale non progressive avec séquences de Moebius et de Robin fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5834741000241118 syndrome de Carey-Fineman-Ziter fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5834731000241111 myopathie congénitale non progressive avec séquences de Moebius et de Robin fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5834741000241118 syndrome de Carey-Fineman-Ziter fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3383211001000115 Carey-Fineman-Ziter-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
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Is a Congenital anomaly of skeletal muscle (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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