Search for a rare disease
Other search option(s)
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


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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.