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720818003: Craniosynostosis Philadelphia type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3322174015 Craniosynostosis Philadelphia type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3322175019 Craniosynostosis Philadelphia type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402485015 Craniosynostosis, Philadelphia type is a form of syndromic craniosynostosis, characterized by sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. Craniosynostosis, Philadelphia type has been suggested to share the same etiology as syndactyly type 1A. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402486019 Craniosynostosis, Philadelphia type is a form of syndromic craniosynostosis, characterised by sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. Craniosynostosis, Philadelphia type has been suggested to share the same aetiology as syndactyly type 1A. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322174015 Craniosynostosis Philadelphia type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3322175019 Craniosynostosis Philadelphia type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3322176018 A form of syndromic craniosynostosis with characteristics of sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402485015 Craniosynostosis, Philadelphia type is a form of syndromic craniosynostosis, characterized by sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. Craniosynostosis, Philadelphia type has been suggested to share the same etiology as syndactyly type 1A. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402486019 Craniosynostosis, Philadelphia type is a form of syndromic craniosynostosis, characterised by sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. Craniosynostosis, Philadelphia type has been suggested to share the same aetiology as syndactyly type 1A. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3447291001000117 Kraniosynostose Typ Philadelphia de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
936651000172119 craniosynostose type Philadelphie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
936651000172119 craniosynostose type Philadelphie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3447291001000117 Kraniosynostose Typ Philadelphia de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Craniosynostosis Philadelphia type (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Acrocephalosyndactyly false Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniosynostosis Philadelphia type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniosynostosis Philadelphia type (disorder) Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniosynostosis Philadelphia type (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniosynostosis Philadelphia type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniosynostosis Philadelphia type (disorder) Finding site Digit structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Craniosynostosis Philadelphia type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniosynostosis Philadelphia type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniosynostosis Philadelphia type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniosynostosis Philadelphia type (disorder) Finding site Digit structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniosynostosis Philadelphia type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniosynostosis Philadelphia type (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
Craniosynostosis Philadelphia type (disorder) Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniosynostosis Philadelphia type (disorder) Is a Disease of skull false Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Syndactyly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Congenital anomaly of bone and joint true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Is a Congenital abnormality of skull shape true Inferred relationship Existential restriction modifier (core metadata concept)
Craniosynostosis Philadelphia type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniosynostosis Philadelphia type (disorder) Associated morphology Abnormal shape (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Craniosynostosis Philadelphia type (disorder) Associated morphology Premature fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Craniosynostosis Philadelphia type (disorder) Associated morphology Abnormally fused structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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