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: -
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: -

Summary

This disease is described under Rare non-syndromic intellectual disability

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 (2021) - GeneReviews
English (2022) - GeneReviews
English (2023) - GeneReviews

Genetic Testing

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

produced/endorsed by ERN(s) FSMR

produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Eurordis directory

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.