Orphanet: Autosomal dominant non syndromic intellectual disability

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Autosomal dominant non-syndromic intellectual disability

ORPHA:178469

Classification level: Subtype of disorder

Synonym(s): -
Prevalence: -
Inheritance: Autosomal dominant
Age of onset: Infancy, Childhood
ICD-10: F70 F71 F72 F73
ICD-11: LD90.Y
OMIM: 156200 612580 612581 612621 613970 614113 614254 614255 614256 614257 614563 615828 616083 616393 616579 616977 617796 617798 617799 617854 618095 618106 618330 619188 620114 620157
UMLS: C5680502
MeSH: -
GARD: 12107
MedDRA: -

Detailed information

General public

Article for general public
Georgian (2018, pdf) - Unique
English (2020, pdf) - Unique
Russian (2020, pdf) - Unique
Russian (2021, pdf) - Unique
Türkçe (2022, pdf) - Unique

Guidelines

Clinical practice guidelines
Deutsch (2015) - AWMF

Disease review articles

Clinical genetics review
English (2019) - GeneReviews
English (2021) - GeneReviews
English (2022) - GeneReviews
English (2023) - GeneReviews
English (2023) - GeneReviews

Genetic Testing

Guidance for genetic testing
Français (2016, pdf) - ANPGM

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Autosomal dominant non-syndromic intellectual disability

ORPHA:178469

Summary

General public

Guidelines

Disease review articles

Genetic Testing

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services