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778006008: Autosomal dominant aplasia and myelodysplasia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3736387018 Autosomal dominant aplasia and myelodysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3736388011 Autosomal dominant aplasia and myelodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3736389015 Autosomal dominant aplastic anaemia and myelodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3736390012 Autosomal dominant aplastic anemia and myelodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3736391011 A rare genetic haematologic disorder characterised by bone marrow failure which manifests with aplastic anaemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3736392016 A rare genetic hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner. Caused by heterozygous mutation in the SRP72 gene on chromosome 4q12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia (disorder) Occurrence Congenital true Inferred relationship Some 2
Autosomal dominant aplasia and myelodysplasia (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Autosomal dominant aplasia and myelodysplasia (disorder) Finding site Bone marrow structure true Inferred relationship Some 1
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Autosomal dominant aplasia and myelodysplasia (disorder) Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Bone marrow disorder true Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Congenital deafness true Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia (disorder) Finding site Inner ear structure (body structure) true Inferred relationship Some 2
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Congenital anomaly of inner ear true Inferred relationship Some
Autosomal dominant aplasia and myelodysplasia (disorder) Interprets Hearing true Inferred relationship Some 3
Autosomal dominant aplasia and myelodysplasia (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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