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47516005: Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (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
79213017 Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
784983015 Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
79213017 Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
784983015 Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6239901000241111 sphérocytose héréditaire due à un déficit combiné en spectrine et en ankyrine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6239901000241111 sphérocytose héréditaire due à un déficit combiné en spectrine et en ankyrine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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