FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

720612000: Cardiospondylocarpofacial syndrome (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
3321537011 Cardiospondylocarpofacial syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3321538018 Cardiospondylocarpofacial syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3321539014 Forney syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321540011 Forney Robinson Pascoe syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3321541010 Mitral regurgitation with deafness and skeletal anomalies 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
Cardiospondylocarpofacial syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Conductive hearing loss true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Mitral valve regurgitation false Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Short stature disorder true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Finding site Ear structure false Inferred relationship Existential restriction modifier 4
Cardiospondylocarpofacial syndrome Interprets Hearing, function false Inferred relationship Existential restriction modifier 3
Cardiospondylocarpofacial syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Associated morphology Valvular insufficiency false Inferred relationship Existential restriction modifier 5
Cardiospondylocarpofacial syndrome Finding site Mitral valve structure false Inferred relationship Existential restriction modifier 5
Cardiospondylocarpofacial syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
Cardiospondylocarpofacial syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Cardiospondylocarpofacial syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 6
Cardiospondylocarpofacial syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Cardiospondylocarpofacial syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Cardiospondylocarpofacial syndrome Associated morphology Valvular insufficiency true Inferred relationship Existential restriction modifier 1
Cardiospondylocarpofacial syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Cardiospondylocarpofacial syndrome Finding site Mitral valve structure true Inferred relationship Existential restriction modifier 1
Cardiospondylocarpofacial syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Cardiospondylocarpofacial syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Cardiospondylocarpofacial syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Interprets Height / growth measure false Inferred relationship Existential restriction modifier 5
Cardiospondylocarpofacial syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 6
Cardiospondylocarpofacial syndrome Interprets Cardiac function true Inferred relationship Existential restriction modifier 6
Cardiospondylocarpofacial syndrome Is a Congenital insufficiency of mitral valve true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Cardiospondylocarpofacial syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Cardiospondylocarpofacial syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 4
Cardiospondylocarpofacial syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 3
Cardiospondylocarpofacial syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Cardiospondylocarpofacial syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 5
Cardiospondylocarpofacial syndrome Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier
Cardiospondylocarpofacial syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Cardiospondylocarpofacial syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 5
Cardiospondylocarpofacial syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start