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Diseases
Genes (426)
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APP
Cerebral Amyloid Angiopathy, App-Related
Neurogenic Inflammation
Inclusion Body Myositis
Fraxe Intellectual Disability
Hereditary Cerebral Amyloid Angiopathy
Familial Amyloid Polyneuropathy
Seborrheic Keratosis
AFF2
Fraxe Intellectual Disability
TTR
Primary Cutaneous Amyloidosis
Inclusion Body Myositis
Familial Amyloid Polyneuropathy
TNF
Pustular Psoriasis
Hyperacusis
Eating Disorder
Neurogenic Inflammation
Seborrheic Keratosis
PIK3CA
Seborrheic Keratosis
IL36RN
Pustular Psoriasis
PHOX2B
Central Hypoventilation Syndrome
ADAM10
Alzheimer Disease 18
RET
Primary Cutaneous Amyloidosis
Color Blindness
Central Hypoventilation Syndrome
IL31RA
Primary Cutaneous Amyloidosis
TACR1
Neurogenic Inflammation
TAC1
Neurogenic Inflammation
GPC4
Nasodigitoacoustic Syndrome
ASCL1
Central Hypoventilation Syndrome
FGFR3
Seborrheic Keratosis
OSMR
Primary Cutaneous Amyloidosis
SERPING1
Angioedema Induced By Ace Inhibitors, Susceptibility To
KNG1
Angioedema Induced By Ace Inhibitors, Susceptibility To
CNGA3
Color Blindness
PDE6H
Color Blindness