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715531000: Tibial aplasia and ectrodactyly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302940010 Tibial aplasia and ectrodactyly syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302941014 Tibial aplasia and ectrodactyly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3302942019 Aplasia of tibia with split hand split foot deformity en Synonym Active Entire term case insensitive SNOMED CT core module
3302943012 Tibial hemimelia ectrodactyly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3302944018 Split hand foot malformation with long bone deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tibial aplasia and ectrodactyly syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Is a Ectrodactyly true Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Is a Congenital anomaly of tibia false Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 2
Tibial aplasia and ectrodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Tibial aplasia and ectrodactyly syndrome Finding site Entire digit true Inferred relationship Existential restriction modifier 2
Tibial aplasia and ectrodactyly syndrome Associated morphology Aplasia false Inferred relationship Existential restriction modifier 3
Tibial aplasia and ectrodactyly syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Tibial aplasia and ectrodactyly syndrome Finding site Bone structure of tibia false Inferred relationship Existential restriction modifier 3
Tibial aplasia and ectrodactyly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Tibial aplasia and ectrodactyly syndrome Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Tibial aplasia and ectrodactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Tibial aplasia and ectrodactyly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Tibial aplasia and ectrodactyly syndrome Finding site Bone structure of tibia true Inferred relationship Existential restriction modifier 1
Tibial aplasia and ectrodactyly syndrome Associated morphology Absence true Inferred relationship Existential restriction modifier 2
Tibial aplasia and ectrodactyly syndrome Is a Absence of tibia false Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Tibial aplasia and ectrodactyly syndrome Is a Congenital absence of tibia 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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