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720606005: Cardiocranial syndrome Pfeiffer type (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3321520016 Cardiocranial syndrome Pfeiffer type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3321521017 Cardiocranial syndrome Pfeiffer type en Synonym Active Only initial character case insensitive SNOMED CT core module
3321522012 Craniosynostosis with congenital heart disease and intellectual disability syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3321523019 Pfeiffer Singer Zschiesche syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321524013 Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis 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
Cardiocranial syndrome Pfeiffer type Is a Congenital heart disease true Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Congenital anomaly of skull false Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Congenital anomaly of bone and joint false Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Developmental delay true Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Cardiocranial syndrome Pfeiffer type Associated morphology Congenital premature fusion false Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Finding site Structure of sagittal suture of skull false Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Cardiocranial syndrome Pfeiffer type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Cardiocranial syndrome Pfeiffer type Finding site Heart structure false Inferred relationship Existential restriction modifier 3
Cardiocranial syndrome Pfeiffer type Finding site Heart structure true Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Cardiocranial syndrome Pfeiffer type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Cardiocranial syndrome Pfeiffer type Finding site Structure of sagittal suture of skull true Inferred relationship Existential restriction modifier 1
Cardiocranial syndrome Pfeiffer type Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 1
Cardiocranial syndrome Pfeiffer type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Cardiocranial syndrome Pfeiffer type Is a Developmental hereditary disorder 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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