700062000: Schöpf-Schulz-Passarge syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Schöpf-Schulz-Passarge syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

2988985014 Schöpf-Schulz-Passarge syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2988996018 Schöpf-Schulz-Passarge syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

871071000172118 SSPS - Schöpf-Schulz-Passarge syndrome fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)

943791000172114 syndrome de Schöpf-Schulz-Passarge fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

911241000172115 syndroom van Schöpf-Schulz-Passarge nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

1004671000172119 eccriene tumoren, ectodermale dysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Schöpf-Schulz-Passarge syndrome	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Some

Inbound Relationships

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This concept is not in any reference sets