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725096002: Cryptomicrotia brachydactyly syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3438493012 Cryptomicrotia brachydactyly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438494018 Cryptomicrotia brachydactyly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438495017 Cryptomicrotia, brachydactyly, excess fingertip arch syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438496016 Tonoki Ohura Niikawa syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403389018 A rare genetic, congenital malformation syndrome characterized by the combination bilateral cryptomicrotia, brachytelomesophalangy with short middle and distal phalanges of digits 2 through 5, hypoplastic toenails and excess fingertip arch patterns. There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403390010 A rare genetic, congenital malformation syndrome characterised by the combination bilateral cryptomicrotia, brachytelomesophalangy with short middle and distal phalanges of digits 2 through 5, hypoplastic toenails and excess fingertip arch patterns. There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3438493012 Cryptomicrotia brachydactyly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438494018 Cryptomicrotia brachydactyly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438495017 Cryptomicrotia, brachydactyly, excess fingertip arch syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438496016 Tonoki Ohura Niikawa syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3438497013 This syndrome describes a combination of malformations that include bilateral cryptomicrotia (recessed, hidden and small or absent ears), brachytelomesophalangy with short middle and distal phalanges of digits two through five, hypoplastic toenails and excess fingertip arch patterns. The syndrome has been reported in one family (mother and son). There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403389018 A rare genetic, congenital malformation syndrome characterized by the combination bilateral cryptomicrotia, brachytelomesophalangy with short middle and distal phalanges of digits 2 through 5, hypoplastic toenails and excess fingertip arch patterns. There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403390010 A rare genetic, congenital malformation syndrome characterised by the combination bilateral cryptomicrotia, brachytelomesophalangy with short middle and distal phalanges of digits 2 through 5, hypoplastic toenails and excess fingertip arch patterns. There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3437531001000119 Kryptomikrotie - Brachydaktylie - Anomalie der Dermatoglyphen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5866011000241117 syndrome de cryptomicrotie et brachydactylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5866011000241117 syndrome de cryptomicrotie et brachydactylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437531001000119 Kryptomikrotie - Brachydaktylie - Anomalie der Dermatoglyphen 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
Cryptomicrotia brachydactyly syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Is a Brachymesophalangia true Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Is a Congenital abnormality of external ear true Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Cryptomicrotia brachydactyly syndrome Associated morphology Abnormally short growth false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cryptomicrotia brachydactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cryptomicrotia brachydactyly syndrome Finding site Entire phalanx false Inferred relationship Existential restriction modifier (core metadata concept) 2
Cryptomicrotia brachydactyly syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cryptomicrotia brachydactyly syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cryptomicrotia brachydactyly syndrome Finding site External ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Cryptomicrotia brachydactyly syndrome Finding site External ear structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cryptomicrotia brachydactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cryptomicrotia brachydactyly syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cryptomicrotia brachydactyly syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cryptomicrotia brachydactyly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Cryptomicrotia brachydactyly syndrome Finding site Entire phalanx false Inferred relationship Existential restriction modifier (core metadata concept) 1
Cryptomicrotia brachydactyly syndrome Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cryptomicrotia brachydactyly syndrome Finding site Entire middle phalanx (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Cryptomicrotia brachydactyly syndrome 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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