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Diseases
Genes (881)
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TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
UBA1
X-Linked Spinal Muscular Atrophy Type 2
FLNA
Subglottic Stenosis
Intestinal Neuronal Dysplasia
Fg Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Dural Arteriovenous Fistula
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
HRAS
Subglottic Stenosis
Adenoid Cystic Carcinoma
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
CTNS
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma