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733118006: Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3498796018 Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3498797010 Johnson Munson syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3498798017 Aphalangy, hemivertebra, urogenital, intestinal dysgenesis 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
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Congenital hemivertebra true Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Congenital absence of skeletal bone false Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Adactyly true Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Aplasia true Inferred relationship Existential restriction modifier 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Finding site Bone structure of spine true Inferred relationship Existential restriction modifier 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 3
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Finding site Phalanx structure false Inferred relationship Existential restriction modifier 3
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Finding site Phalanx structure true Inferred relationship Existential restriction modifier 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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