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770755007: Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3702468014 MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3 en Synonym Active Case sensitive SNOMED CT core
3702469018 Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency en Synonym Active Initial character case insensitive SNOMED CT core
3702470017 Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome en Synonym Active Case insensitive SNOMED CT core
3702471018 Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3702472013 Congenital disorder of glycosylation due to PIGT deficiency en Synonym Active Initial character case insensitive SNOMED CT core
3702473015 A rare congenital disorder of glycosylation with characteristics of neonatal hypotonia, global development delay, developmental regress and severe to profound intellectual disability, infantile onset seizures that are initially associated with febrile episodes with subsequent transition to unprovoked seizures, impaired vision with esotropia and nystagmus, progressive cerebral and cerebellar atrophy, skeletal abnormalities (including brachycephaly, scoliosis, slender long bones, delayed bone age, pectus excavatum and osteopenia), inverted nipples and dysmorphic features including high and narrow forehead, frontal bossing, short nose, depressed nasal bridge, anteverted nares, high palate and wide open mouth consistent with facial hypotonia. Other features may include cardiac abnormalities (such as patent ductus arteriosus, atrial septal defects), urogenital abnormalities (such as nephrocalcinosis, urolithiasis), and low plasma concentration of alkaline phosphatase. There is evidence the disease is caused by homozygous or compound heterozygous mutation in the PIGT gene on chromosome 20q13. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Interprets Intellectual ability true Inferred relationship Some 4
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Has interpretation Impaired true Inferred relationship Some 4
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Interprets Adaptation behaviour true Inferred relationship Some 5
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Has interpretation Impaired true Inferred relationship Some 5
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Inherited metabolic disorder of nervous system true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Hereditary disorder of nervous system false Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Finding site Bone structure true Inferred relationship Some 1
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Intellectual disability true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Some 1
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Metabolic bone disease true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Some 2
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Congenital skeletal dysplasia true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Carbohydrate deficient glycoprotein syndrome true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Occurrence Congenital true Inferred relationship Some 3
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 1
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Is a Seizure disorder true Inferred relationship Some
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Finding site Face structure true Inferred relationship Some 3
Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome Finding site Brain structure true Inferred relationship Some 2

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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