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88456007: Congenital partial absence (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    146668017 Congenital partial absence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    146669013 Partial agenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    831143011 Congenital partial absence (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    146668017 Congenital partial absence en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    146668017 Congenital partial absence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    146669013 Partial agenesis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    146669013 Partial agenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    831143011 Congenital partial absence (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    831143011 Congenital partial absence (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital partial absence Is a Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Cleft hand - central (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Partial agenesis of corpus callosum Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Partial aphalangia of upper limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    amélie d'un membre supérieur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Phocomelia of upper limb NOS Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hypoplasia of corpus callosum Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 4
    Phocomelia of upper limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Complete phocomelia of upper limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    hémimélie d'un membre supérieur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Partial aphalangia of lower limb (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Cleft hand - first cleft Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Cleft hand with polydactyly Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital amputation of upper limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    bras rudimentaire Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital cleft hand Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Amelia of lower limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Transverse deficiency lower limb - through femur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    hémimélie d'un membre inférieur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Transverse deficiency lower limb - knee level Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    hémimélie d'un membre inférieur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    hémimélie Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Transverse deficiency of lower limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital absence of part of upper limb (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital absence of part of upper arm Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Duane-radial ray syndrome Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 7
    Congenital hypodontia, multiple teeth, related to systemic disease Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hypodontia and nail dysgenesis Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Partial congenital absence of teeth (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Familial hypodontia Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 5
    Congenital hypodontia, multiple teeth, unrelated to systemic disease Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Amelia of lower limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Partial congenital absence of limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Transverse deficiency of lower limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Transverse deficiency of arm, upper arm level - long (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Transverse deficiency lower limb - through femur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Transverse deficiency of arm, upper arm level - short Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Transverse deficiency lower limb - knee level Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    hémimélie Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Transverse deficiency lower limb - metatarsal level Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital partial absence of alimentary tract Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    hémimélie d'un membre supérieur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Partial radial absence Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    hémimélie d'un membre inférieur Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Transverse deficiency lower limb - through tibia/fibula Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    anomalie transverse du bras au niveau de l'avant-bras Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Duane-radial ray syndrome Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 1
    Transverse deficiency of upper limb Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Acephalostomia (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Incomplete congenital absence of thigh AND leg Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Incomplete congenital absence of thigh AND leg Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 4
    Partial aphalangia of lower limb (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital tibial deficiency type III Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital tibial deficiency type II Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita due to teratogenic drug (Type 7) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita associated with fetus papyraceus (Type 5) (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis in Johanson-Blizzard syndrome (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita due to underlying malformation (Type 4) (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Adams-Oliver syndrome Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Congenital absence of skin on scalp with epidermal nevi Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita following intra-uterine infection (Type 8) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Congenital absence of skin on scalp Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 3
    Aplasia cutis in Trisomy 13 syndrome Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2
    Oculocerebrocutaneous syndrome (disorder) Associated morphology False Congenital partial absence Inferred relationship Existential restriction modifier (core metadata concept) 2

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    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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