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Lipodystrophy, partial, acquired, with low complement component C3, with or without glomerulonephritis

International Division

Monday-Friday :
8.30 am - 6.30 pm (GMT + 1)
T. : +33 4 72 80 23 85
Contact by email

Disease code:

OMIM:613913

Associated therapeutic area(s):

Abnormality of the genitourinary system (HP:0000119)
Abnormality of head or neck (HP:0000152)
Abnormality of metabolism/homeostasis (HP:0001939)
Abnormality of the immune system (HP:0002715)
Abnormality of the musculoskeletal system  (HP:0033127)

Prenalytics:

5 mL whole blood or DNA sample
Room temperature

Turnaround time:

4 semaines

Options available :

Panel
Panel + CNV
Exome
Exome + CNV

Documents to download:

Specific request form: Rare diseases
Specific request form : Exome
"Whole Exome Sequencing" brochure

Important

You have the possibility to add isolated genes in addition to your selection, directly on the test request form.