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778006008: Autosomal dominant aplasia and myelodysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3736387018 Autosomal dominant aplasia and myelodysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3736388011 Autosomal dominant aplasia and myelodysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3736389015 Autosomal dominant aplastic anaemia and myelodysplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3736390012 Autosomal dominant aplastic anemia and myelodysplasia 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
Autosomal dominant aplasia and myelodysplasia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant aplasia and myelodysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Autosomal dominant aplasia and myelodysplasia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant aplasia and myelodysplasia Finding site Bone marrow structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant aplasia and myelodysplasia Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant aplasia and myelodysplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Autosomal dominant aplasia and myelodysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant aplasia and myelodysplasia Is a Bone marrow disorder true Inferred relationship Existential restriction modifier
Autosomal dominant aplasia and myelodysplasia Is a Congenital deafness true Inferred relationship Existential restriction modifier
Autosomal dominant aplasia and myelodysplasia Finding site Inner ear structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant aplasia and myelodysplasia Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier
Autosomal dominant aplasia and myelodysplasia Is a Congenital anomaly of inner ear true Inferred relationship Existential restriction modifier
Autosomal dominant aplasia and myelodysplasia Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Autosomal dominant aplasia and myelodysplasia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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