57863006: Acid phosphatase deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Acid phosphatase deficiency

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Disorder of lysosomal enzyme\Acid phosphatase deficiency

\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Acid phosphatase deficiency
\Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Acid phosphatase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

96212015 Acid phosphatase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

796532014 Acid phosphatase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acid phosphatase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Acid phosphatase deficiency	Is a	Disorder of lysosomal enzyme	true	Inferred relationship	Some
Acid phosphatase deficiency	Is a	Disorder of phosphate, calcium and vitamin D metabolism	true	Inferred relationship	Some
Acid phosphatase deficiency	Occurrence	Congenital	true	Inferred relationship	Some	1
Acid phosphatase deficiency	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets