Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0013144
Disease: Drowsiness
Drowsiness
31 0 1 3.1E-02 0 0
CUI: C0019880
Disease: Homocystinuria
Homocystinuria
39 0 1 2.5E-02 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
85 0 2 2.4E-02 0 0
CUI: C0751434
Disease: Classical phenylketonuria
Classical phenylketonuria
42 0 1 2.3E-02 0 0
CUI: C0009421
Disease: Comatose
Comatose
78 0 1 1.3E-02 0 0
CUI: C0023380
Disease: Lethargy
Lethargy
160 0 2 1.3E-02 0 0
CUI: C1737329
Disease: Dysmorphism
Dysmorphism
80 0 1 1.2E-02 0 0
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
83 0 1 1.2E-02 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia
102 0 1 9.7E-03 0 0
CUI: C1142533
Disease: Smooth philtrum
Smooth philtrum
105 0 1 9.4E-03 0 0
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE
108 0 1 9.2E-03 0 0
CUI: C0011206
Disease: Delirium
Delirium
110 0 1 9.0E-03 0 0
CUI: C0019061
Disease: Hemolytic-Uremic Syndrome
Hemolytic-Uremic Syndrome
110 0 1 9.0E-03 0 0
CUI: C0234133
Disease: Extrapyramidal sign
Extrapyramidal sign
116 0 1 8.5E-03 0 0
CUI: C0022638
Disease: Ketosis
Ketosis
119 0 1 8.3E-03 0 0
CUI: C0025521
Disease: Inborn Errors of Metabolism
Inborn Errors of Metabolism
119 0 1 8.3E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor
124 0 1 8.0E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 1 6.8E-03 0 0
CUI: C0042963
Disease: Vomiting
Vomiting
303 0 2 6.6E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 2 6.6E-03 0 0
CUI: C1836047
Disease: Long face
Long face
182 0 1 5.5E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia
188 0 1 5.3E-03 0 0
CUI: C0027947
Disease: Neutropenia
Neutropenia
389 0 2 5.1E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead
211 0 1 4.7E-03 0 0
CUI: C0235031
Disease: Neurologic Symptoms
Neurologic Symptoms
233 0 1 4.3E-03 0 0