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Diseases
Genes (760)
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FGFR2
Pfeiffer Syndrome
Acrocephalosyndactylia
TTPA
Familial Isolated Vitamin E Deficiency
FGFR1
Pfeiffer Syndrome
MEGF8
Carpenter Syndrome 1
RAB23
Carpenter Syndrome 1
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TWIST1
Pfeiffer Syndrome
Acrocephalosyndactylia
DMPK
Myotonic Dystrophy
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
TP53
Myotonic Dystrophy
Adenoid Cystic Carcinoma
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
PIK3CA
Adenoid Cystic Carcinoma