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782782004: Autosomal recessive spondylometaphyseal dysplasia Megarbane type (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
3755744018 Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3755745017 Autosomal recessive spondylometaphyseal dysplasia Megarbane type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Is a Spondylometaphyseal dysplasia true Inferred relationship Existential restriction modifier
Autosomal recessive spondylometaphyseal dysplasia Megarbane type Is a Congenital anomaly of skeletal bone 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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