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Diseases
Genes (819)
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ARID1A
Coffin-Siris Syndrome 2
Adenoid Cystic Carcinoma
ARID1B
Coffin-Siris Syndrome 2
TTPA
Familial Isolated Vitamin E Deficiency
SMARCE1
Coffin-Siris Syndrome 2
Adenoid Cystic Carcinoma
SOX11
Coffin-Siris Syndrome 2
Adenoid Cystic Carcinoma
ATR
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
Coffin-Siris Syndrome 2
FLVCR1
Posterior Column Ataxia With Retinitis Pigmentosa
SMARCA2
Coffin-Siris Syndrome 2
Adenoid Cystic Carcinoma
PQBP1
Renpenning's Syndrome
CENPJ
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
SOX4
Coffin-Siris Syndrome 2
Adenoid Cystic Carcinoma
PCNT
Microcephaly And Chorioretinopathy, Autosomal Recessive, 2
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
SMARCB1
Pinealoblastoma
Coffin-Siris Syndrome 2
SMARCA1
Coffin-Siris Syndrome 2
Adenoid Cystic Carcinoma