Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
NAVAJO NEUROHEPATOPATHY
|
0.700 | GeneticVariation | CLINVAR | Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy. | 17694548 | 2007 | |||||
Tinnitus
|
0.700 | CausalMutation | CLINVAR | ||||||||
Skeletal muscle atrophy
|
0.700 | CausalMutation | CLINVAR | ||||||||
Gait imbalance
|
0.700 | CausalMutation | CLINVAR | ||||||||
Headache
|
0.700 | CausalMutation | CLINVAR | ||||||||
Hypesthesia
|
0.700 | CausalMutation | CLINVAR | ||||||||
Distal upper limb muscle weakness
|
0.700 | CausalMutation | CLINVAR | ||||||||
Difficulty standing
|
0.700 | CausalMutation | CLINVAR | ||||||||
NAVAJO NEUROHEPATOPATHY
|
0.700 | CausalMutation | CLINVAR | ||||||||
Progressive muscle weakness
|
0.700 | CausalMutation | CLINVAR | ||||||||
Spasm
|
0.700 | CausalMutation | CLINVAR | ||||||||
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
|
0.700 | CausalMutation | CLINVAR | ||||||||
Scoliosis, unspecified
|
0.700 | CausalMutation | CLINVAR | ||||||||
Blepharoptosis
|
0.700 | CausalMutation | CLINVAR | ||||||||
Anisocoria
|
0.700 | CausalMutation | CLINVAR | ||||||||
Gait, Drop Foot
|
0.700 | CausalMutation | CLINVAR | ||||||||
Distal lower limb muscle weakness
|
0.700 | CausalMutation | CLINVAR | ||||||||
Decreased vibratory sense
|
0.700 | CausalMutation | CLINVAR | ||||||||
Photophobia
|
0.700 | CausalMutation | CLINVAR | ||||||||
Absent reflex
|
0.700 | CausalMutation | CLINVAR | ||||||||
Muscle Weakness
|
0.700 | CausalMutation | CLINVAR | ||||||||
Distal lower limb amyotrophy
|
0.700 | CausalMutation | CLINVAR | ||||||||
Difficulty walking
|
0.700 | CausalMutation | CLINVAR | ||||||||
Broad-based gait
|
0.700 | CausalMutation | CLINVAR | ||||||||
Pain in limb
|
0.700 | CausalMutation | CLINVAR |