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33905008: Hereditary spherocytosis due to deficiency of protein 4.2 (disorder)


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
56605010 Hereditary spherocytosis due to deficiency of protein 4.2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765365019 Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
56605010 Hereditary spherocytosis due to deficiency of protein 4.2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
56605010 Hereditary spherocytosis due to deficiency of protein 4.2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
765365019 Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
765365019 Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6260121000241115 sphérocytose héréditaire due à un déficit en protéine 4.2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6260121000241115 sphérocytose héréditaire due à un déficit en protéine 4.2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Is a Hereditary spherocytosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Finding site Erythrocyte true Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocytosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Defect false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Finding site Entire hematological system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Has definitional manifestation érythropénie false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Finding site Hematopoietic system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Is a Disorder of hematopoietic structure (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Has definitional manifestation Hemolysis false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Associated morphology Spherocyte true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Finding site Hematopoietic system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Interprets Red blood cell count true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Interprets Erythrocyte destruction false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Has interpretation Present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) Interprets Haemolysis true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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