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716740009: Potter sequence cleft lip and palate cardiopathy syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3307378014 Potter sequence cleft lip and palate cardiopathy syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3307379018 Potter sequence cleft lip and palate cardiopathy syndrome en Synonym Active Case sensitive SNOMED CT core
3307380015 Thomas syndrome en Synonym Active Case sensitive SNOMED CT core
3307381016 Thomas syndrome has characteristics of renal anomalies, cardiac malformations and cleft lip or palate. It has been described in six patients. Transmission was suggested to be autosomal recessive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thomas syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Thomas syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Thomas syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Thomas syndrome Occurrence Congenital true Inferred relationship Some 1
Thomas syndrome Finding site Structure of heart true Inferred relationship Some 1
Thomas syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Thomas syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Thomas syndrome Is a Congenital heart disease true Inferred relationship Some
Thomas syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Thomas syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Thomas syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Thomas syndrome Associated morphology Developmental abnormality false Inferred relationship Some 2
Thomas syndrome Occurrence Congenital true Inferred relationship Some 2
Thomas syndrome Finding site Face structure true Inferred relationship Some 2
Thomas syndrome Associated morphology Developmental abnormality false Inferred relationship Some 3
Thomas syndrome Occurrence Congenital false Inferred relationship Some 3
Thomas syndrome Finding site Structure of heart 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

Cardiovascular finding reference set

Problem/Diagnosis reference set

Unit of use quantity reference set

Description inactivation indicator reference set

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