Orphanet: X linked Alport syndrome

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X-linked Alport syndrome

ORPHA:88917

Classification level: Subtype of disorder

Synonym(s): -
Prevalence: 1-9 / 100 000
Inheritance: X-linked dominant
Age of onset: Childhood
ICD-10: Q87.8
OMIM: 301050
UMLS: C1567742
MeSH: -
GARD: -
MedDRA: 10001843

Summary

This disease is described under Alport syndrome

Detailed information

Article for general public

Professionals

Guidance for genetic testing
English (2011, pdf)

Clinical genetics review
English (2019)

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.

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X-linked Alport syndrome

ORPHA:88917

Summary

Article for general public

Professionals

Further information on this disease

Health care resources for this disease

Research activities on this disease

Specialised Social Services