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Diseases
Genes (1254)
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PQBP1
Microlissencephaly
Renpenning's Syndrome
ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
F12
Factor Xii Deficiency
ADAMTS18
Microcornea, Myopic Chorioretinal Atrophy, And Telecanthus
ZFPM2
46,xy Sex Reversal 9
PLN
Cardiomyopathy, Familial Hypertrophic, 18
S100B
Hematoma
MED12
Phyllodes Tumor
Mitral Valve Prolapse
KLHL3
Pseudohypoaldosteronism, Type Iie
IL1B
Systemic Inflammatory Response Syndrome
Alopecia, Androgenetic, 1
Bronchopulmonary Dysplasia
Renpenning's Syndrome
AR
Alopecia, Androgenetic, 1
Phyllodes Tumor
Disinhibition
SRD5A2
Alopecia, Androgenetic, 1
FLNA
Phyllodes Tumor
Mitral Valve Prolapse
Bronchopulmonary Dysplasia
RARA
Phyllodes Tumor
Lymphadenopathy
Bronchopulmonary Dysplasia
TP53
Alopecia, Androgenetic, 1
Phyllodes Tumor
Lymphadenopathy
Bronchopulmonary Dysplasia
PRKAR1A
Systemic Inflammatory Response Syndrome
Alopecia, Androgenetic, 1
Lymphadenopathy
CTLA4
Lymphadenopathy
APOA1
Cerebral Creatine Deficiency
Lymphadenopathy
Familial Isolated Vitamin E Deficiency