702431004: Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Feingold syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2995031014 Feingold syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

2995045015 Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2995323014 Microcephaly-oculo-digito-esophageal-duodenal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2995393016 Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3009702015 Microcephaly-oculo-digito-oesophageal-duodenal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3009804010 Oculo-digito-oesophagoduodenal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3009846018 Oculo-digito-esophagoduodenal syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

7894181000172113 syndrome de Brunner-Winter fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

7894191000172111 syndrome de Feingold fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

11434241000172111 syndrome oculodigito-œsophagoduodénal fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4978521000172117 microcefalie-oculo-digito-oesofageaal-duodenaal syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4978531000172119 syndroom van Feingold nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Feingold syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Feingold syndrome	Is a	Multisystem disorder	false	Inferred relationship	Some

Inbound Relationships

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Active

Source

Characteristic

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This concept is not in any reference sets