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Diseases
Genes (637)
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NAGA
Alpha-N-Acetylgalactosaminidase Deficiency
Alpha-N-Acetylgalactosaminidase Deficiency Type 3
Alpha-N-Acetylgalactosaminidase Deficiency Type 2
Infantile Neuroaxonal Dystrophy
PLA2G6
Infantile Neuroaxonal Dystrophy
TTPA
Familial Isolated Vitamin E Deficiency
NIPBL
Cornelia De Lange Syndrome 3
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
CTC1
Cerebroretinal Microangiopathy With Calcifications And Cysts 1
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RAD21
Cornelia De Lange Syndrome 3
SMC1A
Cornelia De Lange Syndrome 3
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
HDAC8
Fibrous Dysplasia Of Bone
Cornelia De Lange Syndrome 3
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
STN1
Cerebroretinal Microangiopathy With Calcifications And Cysts 1
MYH11
Berdon Syndrome