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720831008: Deficiency of cathepsin D (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3322216019 Deficiency of cathepsin D (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3322217011 Deficiency of cathepsin D en Synonym Active Initial character case insensitive SNOMED CT core
3322218018 Cathepsin D deficiency en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deficiency of cathepsin D Is a Specific enzyme deficiency true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital neuronal ceroid lipofuscinosis Due to True Deficiency of cathepsin D Inferred relationship Some 1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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