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Diseases
Genes (2498)
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AR
Partial Androgen Insensitivity Syndrome
Thyroid Carcinoma, Hurthle Cell
Primary Ovarian Insufficiency
Peripheral Artery Disease
Fibroadenoma
BRAF
Thyroid Carcinoma, Hurthle Cell
Sarcoidosis
HLA-DRB1
Severe Acute Respiratory Syndrome
Thyroid Carcinoma, Hurthle Cell
Primary Ovarian Insufficiency
Sarcoidosis
KRT17
Pachyonychia Congenita
NKX2-1
Thyroid Carcinoma, Hurthle Cell
BTNL2
Sarcoidosis
KRT16
Pachyonychia Congenita
RET
Iron Deficiency
Thyroid Carcinoma, Hurthle Cell
Primary Ovarian Insufficiency
CCDC6
Thyroid Carcinoma, Hurthle Cell
ACE
Severe Acute Respiratory Syndrome
Thyroid Carcinoma, Hurthle Cell
Primary Ovarian Insufficiency
Peripheral Artery Disease
Sarcoidosis
FOXE1
Thyroid Carcinoma, Hurthle Cell
Primary Ovarian Insufficiency
ANXA11
Sarcoidosis
PPARG
Iron Deficiency
Thyroid Carcinoma, Hurthle Cell
Sarcoidosis
TGFB1
Thyroid Carcinoma, Hurthle Cell
Sarcoidosis
Lumbar Spinal Stenosis
SLC29A3
Hypertrichosis
KRT6A
Pachyonychia Congenita
NR5A1
Partial Androgen Insensitivity Syndrome
Primary Ovarian Insufficiency
PAX8
Thyroid Carcinoma, Hurthle Cell
Müllerian Agenesis
IL18
Thyroid Carcinoma, Hurthle Cell
Peripheral Artery Disease
Sarcoidosis
NCOA4
Thyroid Carcinoma, Hurthle Cell