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719021005: DK phocomelia syndrome (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
3313362018 DK phocomelia syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313363011 DK phocomelia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313634018 Von Voss-Cherstvoy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313635017 Phocomelia, thrombocytopenia, encephalocele and urogenital malformation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401931012 Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313362018 DK phocomelia syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313363011 DK phocomelia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313634018 Von Voss-Cherstvoy syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313635017 Phocomelia, thrombocytopenia, encephalocele and urogenital malformation syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313635017 Phocomelia, thrombocytopenia, encephalocele and urogenital malformation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3314615010 A very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities and thrombocytopenia. Less than 15 cases have been reported. The spectrum of upper limb defects varies from radial agenesis and phocomelia to amelia. A meningoencephalocele is constant. The intellectual development may be normal. Pathogenesis and cause of this syndrome are unknown. Parental consanguinity reported in a family suggests an autosomal recessive pattern of inheritance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401931012 Von Voss-Cherstvoy syndrome is a very rare disorder with phocomelia of upper limbs, encephalocele, variable brain anomalies, urogenital abnormalities, and thrombocytopenia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3395031001000116 Von-Voss-Cherstvoy-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6066101000241115 syndrome de von Voss-Cherstvoy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6066111000241118 syndrome de phocomélie, thrombocytopénie, encéphalocèle et malformations urogénitales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6066121000241113 syndrome DK phocomélie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6066101000241115 syndrome de von Voss-Cherstvoy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6066111000241118 syndrome de phocomélie, thrombocytopénie, encéphalocèle et malformations urogénitales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6066121000241113 syndrome DK phocomélie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3395031001000116 Von-Voss-Cherstvoy-Syndrom 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
DK phocomelia syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Is a Encephalocele true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Is a Genitourinary congenital anomalies true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Is a Hereditary thrombocytopenic disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier (core metadata concept) 6
DK phocomelia syndrome (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 6
DK phocomelia syndrome (disorder) Finding site Bone structure of head false Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Finding site Bone structure of cranium true Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 5
DK phocomelia syndrome (disorder) Interprets Platelet count true Inferred relationship Existential restriction modifier (core metadata concept) 5
DK phocomelia syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 7
DK phocomelia syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 7
DK phocomelia syndrome (disorder) Finding site Structure of genitourinary system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 7
DK phocomelia syndrome (disorder) Is a Congenital thrombocytopaenia true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
DK phocomelia syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
DK phocomelia syndrome (disorder) Finding site Structure of genitourinary system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
DK phocomelia syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
DK phocomelia syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
DK phocomelia syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
DK phocomelia syndrome (disorder) Associated morphology Congenital failure of fusion with herniated tissue false Inferred relationship Existential restriction modifier (core metadata concept) 3
DK phocomelia syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier (core metadata concept) 3
DK phocomelia syndrome (disorder) Interprets Hemostatic function true Inferred relationship Existential restriction modifier (core metadata concept) 2
DK phocomelia syndrome (disorder) Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 2
DK phocomelia syndrome (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
DK phocomelia syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 4
DK phocomelia syndrome (disorder) Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
DK phocomelia syndrome (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
DK phocomelia syndrome (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 2
DK phocomelia syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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