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Von Willebrand disease
VWF
Von Willebrand disease type 1
,
Von Willebrand disease type 2A
,
Von Willebrand disease type 2M
,
Von Willebrand disease type 2B
,
Von Willebrand disease type 2N
,
Von Willebrand disease type 3
Centrum Medische Genetica - UZ Antwerpen
Macrozoospermia (AURKC gene)
AURKC
Male infertility due to large-headed multiflagellar polyploid spermatozoa
Centrum Medische Genetica - UZ Brussel VUB
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)
AIRE
Autoimmune polyendocrinopathy type 1
Centrum Menselijke Erfelijkheid - KUL
Hyperthyroidism ( familial gestational or familial nonautoimmune, hypothyroidism, thyrotropin) - TSHR
TSHR
Familial hyperthyroidism due to mutations in TSH receptor
,
Hypothyroidism due to TSH receptor mutations
,
Familial gestational hyperthyroidism
Centre de Génétique Humaine - Erasme ULB
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