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1162976004: X-linked recessive hereditary disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4592775017 X-linked recessive hereditary disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4592776016 X-linked recessive hereditary disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

224 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked recessive hereditary disease Is a X-linked hereditary disease true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Androgen resistance syndrome Is a True X-linked recessive hereditary disease Inferred relationship Some
MECP2 duplication syndrome Is a True X-linked recessive hereditary disease Inferred relationship Some
Hemophilia B Leyden (disorder) Is a True X-linked recessive hereditary disease Inferred relationship Some
X-linked common variable immunodeficiency due to SH3 domain containing kinase binding protein 1 deficiency (disorder) Is a True X-linked recessive hereditary disease Inferred relationship Some
X-linked combined immunodeficiency due to SASH3 deficiency Is a True X-linked recessive hereditary disease Inferred relationship Some

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This concept is not in any reference sets

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