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Diseases
Genes (1674)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Renpenning's Syndrome
Fg Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
COL2A1
Osteopetrosis And Related Disorders
Collagen, Type Ii, Alpha-1
BRAF
Thyroid Cancer, Nonmedullary, 1
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
NKX2-1
Thyroid Cancer, Nonmedullary, 1
ACTG2
Osteopetrosis And Related Disorders
Berdon Syndrome
CLCN7
Osteopetrosis And Related Disorders
TNFSF11
Osteopetrosis And Related Disorders
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
PAH
Phenylketonuria
CCDC6
Thyroid Cancer, Nonmedullary, 1
RET
Thyroid Cancer, Nonmedullary, 1
PLEKHM1
Osteopetrosis And Related Disorders
TNFRSF11A
Osteopetrosis And Related Disorders