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Diseases
Genes (671)
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TBC1D24
Doors Syndrome
Doors Syndrome
FMR1
Disinhibition
Fragile X-Associated Tremor/ataxia Syndrome
FECH
Erythropoietic Protoporphyria
UBE3B
Doors Syndrome
Oculocerebrofacial Syndrome, Kaufman Type
FLVCR2
Proliferative Vasculopathy And Hydranencephaly-Hydrocephaly Syndrome
SRPX2
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked
GRIN2D
Epileptic Encephalopathy, Early Infantile, 46
PYCR2
Leukodystrophy, Hypomyelinating, 10
BTC
Otitis Media
Erythropoietic Protoporphyria
FAM155A
Diverticulitis
HBB
Hemoglobin E
TNF
Otitis Media
Subacromial Bursitis
Cholesteatoma
Peritonitis
Muscle Contracture
IL6
Otitis Media
Fibrous Dysplasia Of Bone
Subacromial Bursitis
Diverticulitis
Gastrointestinal Perforation
RSPH4A
Otitis Media
A2ML1
Otitis Media
IL1B
Otitis Media
Subacromial Bursitis
Cholesteatoma
Muscle Contracture
IFNG
Otitis Media
Peritonitis
EREG
Cholesteatoma
Erythropoietic Protoporphyria
AREG
Cholesteatoma
Erythropoietic Protoporphyria
ITGB2
Otitis Media
Congenital Disorder Of Glycosylation, Type Iic