FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

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


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

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 SNOMED CT core module
2694575011 Congenital nonprogressive myopathy with Moebius and Robin sequences en Synonym Active Only initial character case insensitive SNOMED CT core module
2695275018 Carey Fineman Ziter syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nonprogressive myopathy with Moebius and Robin sequences Is a Congenital anomaly of skeletal muscle true Inferred relationship Existential restriction modifier
Congenital nonprogressive myopathy with Moebius and Robin sequences Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Congenital nonprogressive myopathy with Moebius and Robin sequences Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital nonprogressive myopathy with Moebius and Robin sequences Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Congenital nonprogressive myopathy with Moebius and Robin sequences Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Congenital nonprogressive myopathy with Moebius and Robin sequences Finding site Face structure true Inferred relationship Existential restriction modifier 2
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Congenital nonprogressive myopathy with Moebius and Robin sequences Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital nonprogressive myopathy with Moebius and Robin sequences Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital nonprogressive myopathy with Moebius and Robin sequences Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start