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Diseases
Genes (1631)
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COL6A1
Bethlem Myopathy
Down Syndrome
ASL
Argininosuccinic Aciduria
FMR1
Disinhibition
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Down Syndrome
Fg Syndrome
SALL4
Duane-Radial Ray Syndrome
GJA1
Oculodentodigital Dysplasia
Down Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
ACADVL
Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
PMM2
Pmm2 Deficiency
MMUT
Methylmalonyl-Coa Mutase Deficiency
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
TNFAIP3
Haploinsufficiency Of A20
COL6A2
Bethlem Myopathy
Down Syndrome
SLC17A5
Salla Disease
COL6A3
Bethlem Myopathy
Down Syndrome
PQBP1
Renpenning's Syndrome
RECQL4
Baller–gerold Syndrome
Down Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome