Terminology chevron_right Descriptions chevron_right 3726019012 - Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinaemia (en)

Component

3726019012

The component that hold information about this description.

Concept

773730002 |Osteopetrosis hypogammaglobulinemia syndrome (disorder)|

Identifies the concept to which this description applies. Set to the identifier of a concept with id 138875005

Language Code

en

Specifies the language of the description text using the two character ISO-639-1 code. Note that this specifies a language level only, not a dialect or country code.

Type

900000000000013009 |Synonym (core metadata concept)|

Identifies whether the description is fully specified name a synonym or other description type. This field is set to a child of 900000000000446008

Term

Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinaemia

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Case Significance

900000000000448009 |Entire term case insensitive (core metadata concept)|

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Acceptability

Acceptable