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700057001: Emberger syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2988911010 Emberger syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2988917014 Emberger syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3789196014 Deafness - lymphedema - leukemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3789197017 Deafness - lymphoedema - leukaemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Emberger syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Emberger syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Emberger syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
Emberger syndrome Is a Hereditary lymphedema true Inferred relationship Existential restriction modifier
Emberger syndrome Is a Auditory system hereditary disorder false Inferred relationship Existential restriction modifier
Emberger syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier 1
Emberger syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Emberger syndrome Associated morphology Lymphatic edema true Inferred relationship Existential restriction modifier 2
Emberger syndrome Interprets Hearing, function false Inferred relationship Existential restriction modifier 3
Emberger syndrome Is a Hereditary disorder by system true Inferred relationship Existential restriction modifier
Emberger syndrome Finding site Bone marrow structure true Inferred relationship Existential restriction modifier 1
Emberger syndrome Associated morphology Acute myeloid leukemia with multilineage dysplasia true Inferred relationship Existential restriction modifier 1
Emberger syndrome Is a Acute myeloid leukemia with myelodysplasia-related changes true Inferred relationship Existential restriction modifier
Emberger syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier 2
Emberger syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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