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725030006: Familial scaphocephaly syndrome McGillivray type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3437059016 Familial scaphocephaly syndrome McGillivray type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3437060014 Familial scaphocephaly syndrome McGillivray type en Synonym Active Only initial character case insensitive SNOMED CT core module
3437061013 Scaphocephaly, macrocephaly, maxillary retrusion, intellectual disability syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial scaphocephaly syndrome McGillivray type Is a Scaphycephaly false Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Is a Craniosynostosis syndrome false Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Familial scaphocephaly syndrome McGillivray type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Familial scaphocephaly syndrome McGillivray type Associated morphology Congenital abnormal shape false Inferred relationship Existential restriction modifier 2
Familial scaphocephaly syndrome McGillivray type Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier 2
Familial scaphocephaly syndrome McGillivray type Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier 3
Familial scaphocephaly syndrome McGillivray type Finding site Structure of sagittal suture of skull false Inferred relationship Existential restriction modifier 3
Familial scaphocephaly syndrome McGillivray type Is a Interparietal craniosynostosis true Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Is a Congenital abnormality of skull shape true Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Familial scaphocephaly syndrome McGillivray type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Familial scaphocephaly syndrome McGillivray type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Familial scaphocephaly syndrome McGillivray type Finding site Structure of sagittal suture of skull true Inferred relationship Existential restriction modifier 1
Familial scaphocephaly syndrome McGillivray type Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Familial scaphocephaly syndrome McGillivray type Associated morphology Abnormal shape true Inferred relationship Existential restriction modifier 2
Familial scaphocephaly syndrome McGillivray type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Familial scaphocephaly syndrome McGillivray type Is a Congenital anomaly of bone and joint true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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