FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  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 (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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) est un(e) (attribut) Congenital anomaly of skeletal muscle true Inferred relationship Some
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) est un(e) (attribut) Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) Congenital malformation false Inferred relationship Some
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) survenue (attribut) congénital false Inferred relationship Some
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 3
Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder) localisation d'une constatation (attribut) face true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Back to Start