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773404000: Roifman syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3723412017 Roifman syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3723413010 Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome en Synonym Active Case insensitive SNOMED CT core
3723414016 Roifman syndrome en Synonym Active Case sensitive SNOMED CT core
3723415015 A rare genetic immuno-osseous dysplasia disorder with characteristics of pre and post-natal growth retardation, hypotonia, borderline to moderate intellectual disability, retinal dystrophy, spondyloepiphyseal dysplasia (epiphyseal dysplasia, epiphyses ossification delay, vertebral changes) and skeletal anomalies (brachydactyly, fifth finger clinodactyly). Also associated are humeral immunodeficiency with inability to generate specific antibodies and low circulating B-cells, craniofacial dysmorphism that typically includes microcephaly, hypertelorism, long palpebral fissures, prominent eyelashes, a narrow, tubular, upturned nose with hypoplastic alae nasi, long philtrum and thin upper lip. There is evidence the disease is caused by compound heterozygous mutation in the RNU4ATAC gene on chromosome 2q14. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Roifman syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Roifman syndrome Finding site Bone structure true Inferred relationship Some 1
Roifman syndrome Is a Hereditary disorder of immune system true Inferred relationship Some
Roifman syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Roifman syndrome Is a Immuno-osseous dysplasia true Inferred relationship Some
Roifman syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Roifman syndrome Occurrence Congenital true Inferred relationship Some 2
Roifman syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Roifman syndrome Is a Intellectual disability true Inferred relationship Some
Roifman syndrome Occurrence Congenital true Inferred relationship Some 1
Roifman syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Roifman syndrome Finding site Face structure true Inferred relationship Some 2
Roifman syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Roifman syndrome Pathological process Abnormal immune process true Inferred relationship Some 3
Roifman syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Roifman syndrome Occurrence Congenital true Inferred relationship Some 3
Roifman syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Roifman syndrome Interprets Height / growth measure true Inferred relationship Some 4
Roifman syndrome Interprets Intellectual ability true Inferred relationship Some 5
Roifman syndrome Has interpretation Impaired true Inferred relationship Some 5
Roifman syndrome Interprets Adaptation behaviour true Inferred relationship Some 6
Roifman syndrome Has interpretation Impaired true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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