FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

720498007: Aphalangy and syndactyly with microcephaly 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
3321032013 Aphalangy and syndactyly with microcephaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321033015 Aphalangy and syndactyly with microcephaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402363013 An extremely rare malformation syndrome characterized by the association of partial distal aphalangia with syndactyly, duplication of metatarsal IV, microcephaly, and mild intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402364019 An extremely rare malformation syndrome characterised by the association of partial distal aphalangia with syndactyly, duplication of metatarsal IV, microcephaly, and mild intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321032013 Aphalangy and syndactyly with microcephaly syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321032013 Aphalangy and syndactyly with microcephaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321033015 Aphalangy and syndactyly with microcephaly syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3321033015 Aphalangy and syndactyly with microcephaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321034014 An extremely rare malformation syndrome with characteristics of the association of partial distal aphalangia with syndactyly, duplication of metatarsal IV, microcephaly, and mild intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402363013 An extremely rare malformation syndrome characterized by the association of partial distal aphalangia with syndactyly, duplication of metatarsal IV, microcephaly, and mild intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402364019 An extremely rare malformation syndrome characterised by the association of partial distal aphalangia with syndactyly, duplication of metatarsal IV, microcephaly, and mild intellectual disability. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3389161001000111 Aphalangie-Syndaktylie-Mikrozephalie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5766181000241114 syndrome d'aphalangie syndactylie microcéphalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5766191000241111 syndrome d'aphalangie, de syndactylie et de microcéphalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5766181000241114 syndrome d'aphalangie syndactylie microcéphalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5766191000241111 syndrome d'aphalangie, de syndactylie et de microcéphalie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389161001000111 Aphalangie-Syndaktylie-Mikrozephalie-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
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a microcéphalie false Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Adactyly true Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Syndactyly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Digit structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Digit structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 5
Aphalangy and syndactyly with microcephaly syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 4
Aphalangy and syndactyly with microcephaly syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Digit structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Aphalangy and syndactyly with microcephaly syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aphalangy and syndactyly with microcephaly syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Aphalangy and syndactyly with microcephaly syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Digit structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Aphalangy and syndactyly with microcephaly syndrome (disorder) Is a Congenital microcephaly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Aphalangy and syndactyly with microcephaly syndrome (disorder) Finding site Head structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Aphalangy and syndactyly with microcephaly syndrome (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 4
Aphalangy and syndactyly with microcephaly syndrome (disorder) Interprets Birth head circumference true Inferred relationship Existential restriction modifier (core metadata concept) 4
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Abnormally fused structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aphalangy and syndactyly with microcephaly syndrome (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Back to Start