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Diseases
Genes (1423)
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TTPA
Familial Isolated Vitamin E Deficiency
MED12
Sensorineural Hearing Loss
Fg Syndrome
PDGFRB
Sensorineural Hearing Loss
Primary Familial Brain Calcification
GJB2
Sensorineural Hearing Loss
SLC26A4
Sensorineural Hearing Loss
PQBP1
Renpenning's Syndrome
SLC20A2
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
FLNA
Sensorineural Hearing Loss
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
IFIH1
Singleton Merten Syndrome
PDGFB
Primary Familial Brain Calcification
Apathy
MYH9
Sensorineural Hearing Loss
ASS1
Citrullinemia Type I
GJB3
Sensorineural Hearing Loss
TMC1
Sensorineural Hearing Loss
LHX3
Sensorineural Hearing Loss
COL2A1
Sensorineural Hearing Loss
LRP2
Sensorineural Hearing Loss
Cystinosis
CTNS
Cystinosis
SOX2
Sensorineural Hearing Loss