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Diseases
Genes (1115)
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MED12
Fg Syndrome
Phyllodes Tumor
TBX5
Holt–oram Syndrome
FOXP3
Ipex Syndrome
Phyllodes Tumor
TTPA
Familial Isolated Vitamin E Deficiency
FBN2
Congenital Contractural Arachnodactyly
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
Phyllodes Tumor
FGFR2
Jackson–weiss Syndrome
Congenital Contractural Arachnodactyly
PQBP1
Renpenning's Syndrome
RECQL4
Baller–gerold Syndrome
UMOD
Medullary Cystic Kidney Disease
FAM20A
Enamel-Renal Syndrome
FGFR1
Jackson–weiss Syndrome
Congenital Contractural Arachnodactyly
Phyllodes Tumor
UBA1
X-Linked Spinal Muscular Atrophy Type 2
IFIH1
Singleton Merten Syndrome
OFD1
Orofaciodigital Syndrome 1
ASS1
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TNFSF11
Osteopetrosis
Fibrous Dysplasia Of Bone
CTNS
Cystinosis
CLCN7
Osteopetrosis
SLC4A4
Proximal Renal Tubular Acidosis