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Neurofibromatosis type 1 / Legius syndrome (2 genes)
NF1
,
SPRED1
Neurofibromatosis type 1
,
Legius syndrome
Centrum Menselijke Erfelijkheid - KUL
Neurofibromatosis type I
NF1
Neurofibromatosis type 1
Centre de Génétique Médicale UCL
Neurofibromatosis type 1 / Legius syndrome
NF1
,
SPRED1
Neurofibromatosis type 1
,
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
,
17q11 microdeletion syndrome
,
Legius syndrome
Centrum Medische Genetica - UZ Gent
Chronic granulomatous disease, X-linked
CYBB
Chronic granulomatous disease
,
X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
Centrum Menselijke Erfelijkheid - KUL
Multiple endocrine neoplasia type 2A and 2B / Familial medullary thyroid carcinoma
RET
Multiple endocrine neoplasia type 2B
,
Multiple endocrine neoplasia type 2A
,
Familial medullary thyroid carcinoma
Centrum Menselijke Erfelijkheid - KUL
Multiple Endocrine Neoplasia type 2A and 2B / Familial medullary thyroid carcinoma
RET
Multiple endocrine neoplasia type 2A
,
Multiple endocrine neoplasia type 2B
,
Familial medullary thyroid carcinoma
Centre de Génétique Humaine - Erasme ULB
Multiple Endocrine Neoplasia type 2A and 2B / Familial medullary thyroid carcinoma
RET
Multiple endocrine neoplasia type 2A
,
Multiple endocrine neoplasia type 2B
,
Familial medullary thyroid carcinoma
,
Hirschsprung disease
Centrum Medische Genetica - UZ Gent
Medullary thyroid carcinoma
RET
Medullary thyroid carcinoma (3 genes) - UCL
Familial medullary thyroid carcinoma
Centre de Génétique Médicale UCL
Endometrial cancer (gene panel)
Endometrial Cancer (7 genes) - KUL
Endometrial Cancer
Centrum Menselijke Erfelijkheid - KUL
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