Orphanet: X linked non syndromic intellectual disability

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X-linked non-syndromic intellectual disability

ORPHA:777

Classification level: Subtype of disorder

Synonym(s): -
Prevalence: Unknown
Inheritance: X-linked recessive
Age of onset: Infancy, Childhood
ICD-10: F70 F71 F72 F73
ICD-11: LD90.Y
OMIM: 300046 300047 300062 300115 300143 300210 300271 300324 300355 300372 300387 300419 300428 300433 300436 300454 300498 300505 300518 300558 300705 300716 300802 300803 300844 300848 300849 300850 300851 300852 300919 300928 300978 300983 300984 301013 309530 309549
UMLS: C2931498
MeSH: -
GARD: -
MedDRA: -

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

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Guidelines

Clinical practice guidelines
Deutsch (2015) - AWMF

Disease review articles

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

Genetic Testing

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

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X-linked non-syndromic intellectual disability

ORPHA:777

Summary

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Disease review articles

Genetic Testing

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Newborn screening