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

715434005: Holoprosencephaly craniosynostosis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302612019 Holoprosencephaly craniosynostosis syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302613012 Holoprosencephaly craniosynostosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302614018 Camero Lituania Cohen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302615017 Genoa syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
12721901000172111 syndrome d'holoprosencéphalie et craniosténose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
12721911000172114 syndrome de Gênes fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
12721921000172116 syndrome d'holoprosencéphalie et craniosynostose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
12721931000172118 syndrome de Camero-Lituania-Cohen fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4541021000172113 syndroom van Camero-Lituania-Cohen nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4541031000172111 Camero-Lituania-Cohen-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4541041000172116 syndroom van holoprosencefalie en craniosynostose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Holoprosencephaly craniosynostosis syndrome (disorder) Is a Holoprosencephaly sequence true Inferred relationship Some
Holoprosencephaly craniosynostosis syndrome (disorder) Is a Craniosynostosis syndrome true Inferred relationship Some
Holoprosencephaly craniosynostosis syndrome (disorder) Finding site Bone structure of cranium false Inferred relationship Some
Holoprosencephaly craniosynostosis syndrome (disorder) Associated morphology Congenital premature fusion false Inferred relationship Some 2
Holoprosencephaly craniosynostosis syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Holoprosencephaly craniosynostosis syndrome (disorder) Finding site Joint structure of suture of skull false Inferred relationship Some 2
Holoprosencephaly craniosynostosis syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Holoprosencephaly craniosynostosis syndrome (disorder) Finding site Joint structure of suture of skull true Inferred relationship Some 1
Holoprosencephaly craniosynostosis syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Holoprosencephaly craniosynostosis syndrome (disorder) Associated morphology Congenital premature fusion true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

Back to Start