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Diseases
Genes (387)
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TBC1D24
Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, And Seizures Syndrome
Doors Syndrome
SLC6A8
X-Linked Creatine Transporter Deficiency
ARID1B
Coffin-Siris Syndrome
SLC16A2
Allan-Herndon-Dudley Syndrome
SMS
Snyder-Robinson Syndrome
Müllerian Agenesis
PQBP1
Renpenning's Syndrome
UBE3B
Doors Syndrome
Oculocerebrofacial Syndrome, Kaufman Type
ARID1A
Coffin-Siris Syndrome
NRAS
Ras-Associated Autoimmune Leukoproliferative Disorder
SMARCE1
Coffin-Siris Syndrome
SOX11
Coffin-Siris Syndrome
EDNRB
Abcd Syndrome
KRAS
Ras-Associated Autoimmune Leukoproliferative Disorder
ATP6V1B2
Autosomal Dominant Deafness-Onychodystrophy Syndrome
SLC6A4
Obsessive–compulsive Disorder
WASHC5
Ritscher-Schinzel Syndrome
SMARCB1
Coffin-Siris Syndrome
SMARCA4
Coffin-Siris Syndrome
SMARCA1
Coffin-Siris Syndrome
GLRB
Hyperekplexia