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Diseases
Genes (1357)
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AFG3L2
Spinocerebellar Ataxia Type 28
TTPA
Familial Isolated Vitamin E Deficiency
MED12
Sensorineural Hearing Loss
Fg Syndrome
PDGFRB
Primary Familial Brain Calcification
Sensorineural Hearing Loss
LMNA
Sensorineural Hearing Loss
Pleural Effusion
Limb–girdle Muscular Dystrophy
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Sensorineural Hearing Loss
Fg Syndrome
IFIH1
Singleton Merten Syndrome
GJB2
Sensorineural Hearing Loss
SLC26A4
Sensorineural Hearing Loss
DES
Sensorineural Hearing Loss
Limb–girdle Muscular Dystrophy
ACTG2
Berdon Syndrome
TGM1
Bathing Suit Ichthyosis
TTN
Sensorineural Hearing Loss
Limb–girdle Muscular Dystrophy
SGCG
Limb–girdle Muscular Dystrophy
MYOT
Limb–girdle Muscular Dystrophy
CAV3
Limb–girdle Muscular Dystrophy