FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

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


Status: current, Primitive. 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 Initial character case insensitive SNOMED CT core
2694575011 Congenital nonprogressive myopathy with Moebius and Robin sequences en Synonym Active Initial character case insensitive SNOMED CT core
2695275018 Carey Fineman Ziter syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start