Back to search

Leptin receptor deficiency

Disease code:

OMIM:614963

Associated therapeutic area(s):

Growth abnormality (HP:0001507)
Abnormality of the genitourinary system (HP:0000119)
Abnormality of head or neck (HP:0000152)
Abnormality of the nervous system (HP:0000707)
Abnormality of the endocrine system (HP:0000818)
Abnormality of metabolism/homeostasis (HP:0001939)
Abnormality of the respiratory system (HP:0002086)
Abnormality of the immune system (HP:0002715)
See more

Prenalytics:

5 mL whole blood or DNA sample
Room temperature

Turnaround time:

4 semaines

Options available :

Panel
Panel + CNV
Exome
Exome + CNV

Important

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