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


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3498796018 Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome en Synonym Active Case insensitive SNOMED CT core
3498797010 Johnson Munson syndrome en Synonym Active Case sensitive SNOMED CT core
3498798017 Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3499986013 An extremely rare congenital limb malformation syndrome, described in only 3 patients to date with the association of hypoplasia or aplasia of the hand and foot phalanges, hemivertebrae and various urogenital and/or intestinal abnormalities (i.e. dysgenesis of the urogenital tract and rectum). There have been no further descriptions in the literature since 1991. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Occurrence Congenital true Inferred relationship Some 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Finding site Phalanx structure true Inferred relationship Some 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Congenital absence false Inferred relationship Some 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Absence true Inferred relationship Some 1
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Congenital hemivertebra true Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Congenital absence of skeletal bone false Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Adactyly true Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Inherited disorder of connective tissue false Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Aplasia true Inferred relationship Some 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Occurrence Congenital true Inferred relationship Some 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Finding site Bone structure of spine true Inferred relationship Some 2
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Associated morphology Congenital absence false Inferred relationship Some 3
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Occurrence Congenital false Inferred relationship Some 3
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome Finding site Phalanx structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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