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Diseases
Genes (455)
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TTPA
Familial Isolated Vitamin E Deficiency
FLI1
Paris-Trousseau Syndrome
Jacobsen Syndrome
Vascular Tumor
IFIH1
Dermatopolymyositis
Singleton Merten Syndrome
Jaccoud Arthropathy
PQBP1
Renpenning's Syndrome
KIF2A
Cortical Dysplasia, Complex, With Other Brain Malformations 3
TUBG1
Cortical Dysplasia, Complex, With Other Brain Malformations 4
PHF21A
Potocki–shaffer Syndrome
SLC29A3
Histiocytosis
TNF
Dermatopolymyositis
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Potocki–shaffer Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
DDX58
Dermatopolymyositis
Singleton Merten Syndrome
IL1B
Dermatopolymyositis
Renpenning's Syndrome
EXT2
Potocki–shaffer Syndrome
ALX4
Potocki–shaffer Syndrome
IL1A
Dermatopolymyositis
HLA-B
Dermatopolymyositis
Potocki–shaffer Syndrome
C2
Dermatopolymyositis
C9
Dermatopolymyositis
FH
Fumarase Deficiency
KNG1
Hyperesthesia