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716638009: Longitudinal deficiency of part of limb (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307003012 Longitudinal deficiency of part of limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307004018 Longitudinal deficiency of part of limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307005017 Limb part reduction defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307006016 Reduction deformity of part of limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307003012 Longitudinal deficiency of part of limb (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307003012 Longitudinal deficiency of part of limb (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307004018 Longitudinal deficiency of part of limb en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307004018 Longitudinal deficiency of part of limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307005017 Limb part reduction defect en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307005017 Limb part reduction defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307006016 Reduction deformity of part of limb en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3307006016 Reduction deformity of part of limb en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6046281000241113 hémimélie partielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6046291000241110 raccourcissement congénital d'une partie d'un membre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6046281000241113 hémimélie partielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6046291000241110 raccourcissement congénital d'une partie d'un membre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

125 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Longitudinal deficiency of part of limb (disorder) Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of part of limb (disorder) Is a Disorder of limb false Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of part of limb (disorder) Is a Deformity of limb (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of part of limb (disorder) Associated morphology Abnormal shortening true Inferred relationship Existential restriction modifier (core metadata concept) 1
Longitudinal deficiency of part of limb (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Longitudinal deficiency of part of limb (disorder) Finding site Extremity part true Inferred relationship Existential restriction modifier (core metadata concept) 1
Longitudinal deficiency of part of limb (disorder) Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of part of limb (disorder) Is a Congenital deformity (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of part of limb (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Brachyphalangia Is a False Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
hémimélie d'un membre supérieur Is a False Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of foot Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital undergrowth of partial lower limb Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Brachydactyly type A1 Is a False Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Longitudinal deficiency of part of upper limb (disorder) Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Familial digital arthropathy-brachydactyly is characterised by the association of arthropathy of interphalangeal, metacarpophalangeal and metatarsophalangeal joints with brachydactyly of the middle and distal phalanges. It has been described in numerous members from five generations of one large family. Inheritance is autosomal dominant. Is a False Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital contracture of gastrocnemius muscle (disorder) Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital abduction contracture of hip Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital flexion contracture of knee (disorder) Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital contracture of toe joint Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital extension contracture of the knee Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital flexion contracture of hip Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare syndrome characterised by an arthrogryposis-like hand anomaly and sensorineural deafness. It has been described in only one family. Male-to-male transmission was observed. Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
hémimélie Is a False Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Distal arthrogryposis type 10 Is a False Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome (disorder) Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital flexion contracture of foot joint (disorder) Is a True Longitudinal deficiency of part of limb (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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