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Diseases
Genes (919)
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FMR1
Disinhibition
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
Fg Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
CPT1A
Carnitine Palmitoyltransferase I Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
GNAQ
Sturge–weber Syndrome
CDKN1C
Beckwith-Wiedemann Syndrome
SLC17A5
Salla Disease
NGLY1
Ngly1 Deficiency
FECH
Erythropoietic Protoporphyria
IGF2
Beckwith-Wiedemann Syndrome
H19
Beckwith-Wiedemann Syndrome
KCNQ1OT1
Beckwith-Wiedemann Syndrome
RASA1
Sturge–weber Syndrome
CD55
Protein Losing Enteropathy
KCNQ1
Chronic Periodontitis
Beckwith-Wiedemann Syndrome
IL6
Fibrous Dysplasia Of Bone
Familial Isolated Vitamin E Deficiency
Chronic Periodontitis
Subacromial Bursitis
Uveitis
TNF
Familial Isolated Vitamin E Deficiency
Chronic Periodontitis
Renpenning's Syndrome
Salla Disease
Subacromial Bursitis
Uveitis
NSD1
Beckwith-Wiedemann Syndrome
H19-ICR
Beckwith-Wiedemann Syndrome