Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Intrauterine retardation
|
0.700 | CausalMutation | CLINVAR | ||||||||
Feeding difficulties
|
0.700 | CausalMutation | CLINVAR | ||||||||
Recurrent infections
|
0.700 | CausalMutation | CLINVAR | ||||||||
Decreased vibratory sense
|
0.700 | CausalMutation | CLINVAR | ||||||||
Sleep Apnea, Obstructive
|
0.700 | CausalMutation | CLINVAR | ||||||||
VERVERI-BRADY SYNDROME
|
0.700 | CausalMutation | CLINVAR | ||||||||
Dysautonomia
|
0.700 | CausalMutation | CLINVAR | ||||||||
Progressive inability to walk
|
0.700 | CausalMutation | CLINVAR | ||||||||
Bradycardia
|
0.700 | CausalMutation | CLINVAR | ||||||||
Intermittent painful muscle spasms
|
0.700 | CausalMutation | CLINVAR | ||||||||
Motor delay
|
0.700 | CausalMutation | CLINVAR | ||||||||
Nasal, dysarthic speech
|
0.700 | CausalMutation | CLINVAR | ||||||||
Waddling gait
|
0.700 | CausalMutation | CLINVAR | ||||||||
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
|
0.700 | CausalMutation | CLINVAR | ||||||||
Mitochondrial respiratory chain defects
|
0.700 | CausalMutation | CLINVAR | ||||||||
Decreased muscle mass
|
0.700 | CausalMutation | CLINVAR | ||||||||
Blepharoptosis
|
0.700 | CausalMutation | CLINVAR | ||||||||
Restrictive ventilatory defect
|
0.700 | CausalMutation | CLINVAR | ||||||||
Temperature instability
|
0.700 | CausalMutation | CLINVAR | ||||||||
Muscle Weakness
|
0.700 | CausalMutation | CLINVAR | ||||||||
Decreased tendon reflex
|
0.700 | CausalMutation | CLINVAR | ||||||||
Gastrointestinal dysmotility
|
0.700 | CausalMutation | CLINVAR | ||||||||
Generalized hypotonia
|
0.700 | CausalMutation | CLINVAR | ||||||||
Seizures
|
0.700 | CausalMutation | CLINVAR | ||||||||
Developmental stagnation
|
0.700 | CausalMutation | CLINVAR |