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782941005: Richieri Costa-da Silva syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3756872010 Richieri Costa-da Silva syndrome en Synonym Active Case sensitive SNOMED CT core
3756873017 Myotonia, intellectual disability, skeletal anomalies syndrome en Synonym Active Case insensitive SNOMED CT core
3756874011 Richieri Costa-da Silva syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3756875012 A rare genetic myotonic syndrome characterized by childhood onset of progressive and severe myotonia (with generalized muscular hypertrophy and progressive impairment of gait) short stature, skeletal abnormalities (including pectus carinatum, short, wedge-shaped thoracolumbar vertebrae, kyphoscoliosis, genu valgum, irregular femoral epiphyses) and mild to moderate intellectual deficiency. Facial dysmorphism and joint limitation are not associated. There have been no further descriptions in the literature since 1984. en Definition Active Case sensitive SNOMED CT core
3756876013 A rare genetic myotonic syndrome characterised by childhood onset of progressive and severe myotonia (with generalised muscular hypertrophy and progressive impairment of gait) short stature, skeletal abnormalities (including pectus carinatum, short, wedge-shaped thoracolumbar vertebrae, kyphoscoliosis, genu valgum, irregular femoral epiphyses) and mild to moderate intellectual deficiency. Facial dysmorphism and joint limitation are not associated. There have been no further descriptions in the literature since 1984. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Richieri Costa-da Silva syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Richieri Costa-da Silva syndrome Is a Intellectual disability true Inferred relationship Some
Richieri Costa-da Silva syndrome Is a Metaphyseal chondrodysplasia true Inferred relationship Some
Richieri Costa-da Silva syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Richieri Costa-da Silva syndrome Occurrence Congenital true Inferred relationship Some 2
Richieri Costa-da Silva syndrome Is a Congenital myotonia false Inferred relationship Some
Richieri Costa-da Silva syndrome Finding site Skeletal muscle structure true Inferred relationship Some 2
Richieri Costa-da Silva syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Richieri Costa-da Silva syndrome Occurrence Congenital true Inferred relationship Some 1
Richieri Costa-da Silva syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Richieri Costa-da Silva syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
Richieri Costa-da Silva syndrome Finding site Bone structure true Inferred relationship Some 1
Richieri Costa-da Silva syndrome Is a Myotonic disorder true Inferred relationship Some
Richieri Costa-da Silva syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Richieri Costa-da Silva syndrome Interprets Height / growth measure true Inferred relationship Some 3
Richieri Costa-da Silva syndrome Interprets Intellectual ability true Inferred relationship Some 4
Richieri Costa-da Silva syndrome Has interpretation Impaired true Inferred relationship Some 4
Richieri Costa-da Silva syndrome Interprets Adaptation behaviour true Inferred relationship Some 5
Richieri Costa-da Silva syndrome Has interpretation Impaired true Inferred relationship Some 5

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

Description inactivation indicator reference set

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