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783156008: Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757863014 Hecht Scott syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3757865019 FATCO syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3757868017 Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3757869013 Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Associated morphology Abnormal shortening true Inferred relationship Existential restriction modifier 1
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Is a Longitudinal deficiency of limb true Inferred relationship Existential restriction modifier
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Finding site Entire limb true Inferred relationship Existential restriction modifier 1
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Is a Congenital anomaly of limb false Inferred relationship Existential restriction modifier
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Is a Congenital deformity false Inferred relationship Existential restriction modifier
Fibular aplasia, tibial campomelia, oligo-syndactyly syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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