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725289009: 5-amino-4-imidazolcarboxamideribosidurie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3440760015 5-amino-4-imidazole carboxamide ribosiduria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3440761016 5-amino-4-imidazole carboxamide ribosiduria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3440763018 ATIC (5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase) deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3780959012 AICA (5-amino-4-imidazole carboxamide) ribosiduria en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6796841000146111 5-amino-4-imidazolcarboxamideribosidurie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6796851000146114 AICA-ribosidurie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6796861000146112 5-amino-4-imidazolcarboxamideribosidurie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6905771000146110 ATIC-deficiëntie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3440764012 An extremely severe inborn error of purine biosynthesis with clinical characteristics in the single reported case to date of profound intellectual deficit, epilepsy, dysmorphic features of the knees, elbows and shoulders and congenital blindness. In the one reported case the disease was caused by compound heterozygous mutation in the ATIC gene on chromosome 2q35. 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
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Disorder of purine metabolism true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Congenital anomaly of limb true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a mentale retardatie false Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Hereditary macular dystrophy true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Occurrence Congenital true Inferred relationship Some 2
5-amino-4-imidazole carboxamide ribosiduria (disorder) Finding site Limb structure true Inferred relationship Some 2
5-amino-4-imidazole carboxamide ribosiduria (disorder) Occurrence Congenital false Inferred relationship Some 3
5-amino-4-imidazole carboxamide ribosiduria (disorder) Associated morphology Dystrophy false Inferred relationship Some 2
5-amino-4-imidazole carboxamide ribosiduria (disorder) Finding site Macula lutea structure false Inferred relationship Some 2
5-amino-4-imidazole carboxamide ribosiduria (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 3
5-amino-4-imidazole carboxamide ribosiduria (disorder) Finding site Limb structure false Inferred relationship Some 3
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Intellectual disability true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Occurrence Congenital true Inferred relationship Some 1
5-amino-4-imidazole carboxamide ribosiduria (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Congenital anomaly of macula true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
5-amino-4-imidazole carboxamide ribosiduria (disorder) Finding site Macula lutea structure true Inferred relationship Some 1
5-amino-4-imidazole carboxamide ribosiduria (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
5-amino-4-imidazole carboxamide ribosiduria (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
5-amino-4-imidazole carboxamide ribosiduria (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 3
5-amino-4-imidazole carboxamide ribosiduria (disorder) Has interpretation Impaired true Inferred relationship Some 3
5-amino-4-imidazole carboxamide ribosiduria (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 4
5-amino-4-imidazole carboxamide ribosiduria (disorder) Has interpretation Impaired true Inferred relationship Some 4
5-amino-4-imidazole carboxamide ribosiduria (disorder) Is a Hereditary metabolic disease false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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