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Diseases
Genes (817)
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LCAT
Fish-Eye Disease
TTPA
Familial Isolated Vitamin E Deficiency
RET
Multiple Endocrine Neoplasia Type 2
ANKRD26
Thrombocytopenia 2
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Multiple Endocrine Neoplasia Type 2
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
TP53
Multiple Endocrine Neoplasia Type 2
Myotonic Dystrophy
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis