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702361006: Crouzon-syndroom met acanthosis nigricans (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2995059010 Crouzon syndrome with acanthosis nigricans (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2995457019 Crouzon syndrome with acanthosis nigricans en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3010153011 Crouzonodermoskeletal syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6356731000146115 syndroom van Crouzon met acanthosis nigricans nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6356741000146111 Crouzon-syndroom met acanthosis nigricans nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6356761000146112 CAN nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6356771000146118 crouzonodermoskeletaal syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10664001000146112 Crouzon-syndroom met acanthosis nigricans (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
4022295011 A distinct form of Crouzon disease associated with acanthosis nigricans caused by a specific mutation (p.Ala391Glu) in the transmembrane domain of FGFR3. The disease is transmitted in an autosomal dominant manner with variable penetrance. en Definition 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
Crouzon syndrome with acanthosis nigricans (disorder) Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Is a Acanthosis nigricans (disorder) true Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Is a Crouzon syndrome true Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Skin structure false Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Has definitional manifestation Abnormal keratinization false Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Face structure false Inferred relationship Some 6
Crouzon syndrome with acanthosis nigricans (disorder) Occurrence Congenital false Inferred relationship Some 6
Crouzon syndrome with acanthosis nigricans (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 6
Crouzon syndrome with acanthosis nigricans (disorder) Occurrence Congenital false Inferred relationship Some 5
Crouzon syndrome with acanthosis nigricans (disorder) Associated morphology congenitale premature fusie false Inferred relationship Some 5
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Joint structure of suture of skull false Inferred relationship Some 5
Crouzon syndrome with acanthosis nigricans (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Bone structure of cranium false Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Structure of integumentary system (body structure) true Inferred relationship Some 4
Crouzon syndrome with acanthosis nigricans (disorder) Has interpretation Abnormal true Inferred relationship Some 1
Crouzon syndrome with acanthosis nigricans (disorder) Interprets Keratinization true Inferred relationship Some 1
Crouzon syndrome with acanthosis nigricans (disorder) Associated morphology congenitale premature fusie false Inferred relationship Some 3
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Joint structure of suture of skull true Inferred relationship Some 3
Crouzon syndrome with acanthosis nigricans (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Crouzon syndrome with acanthosis nigricans (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Crouzon syndrome with acanthosis nigricans (disorder) Occurrence Congenital true Inferred relationship Some 3
Crouzon syndrome with acanthosis nigricans (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Crouzon syndrome with acanthosis nigricans (disorder) Occurrence Congenital true Inferred relationship Some 2
Crouzon syndrome with acanthosis nigricans (disorder) Finding site Face structure true Inferred relationship Some 2
Crouzon syndrome with acanthosis nigricans (disorder) Is a Fibroblast growth factor receptor 3-related craniosynostosis (disorder) true Inferred relationship Some
Crouzon syndrome with acanthosis nigricans (disorder) Associated morphology Premature fusion true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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