Source: CLINVAR ×
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: C4317146
Disease: Acid reflux
Acid reflux 		50 58 13 0.17 14 0.15
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		37 41 11 0.17 9 0.11
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		30 46 9 0.15 7 8.0E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		19 23 7 0.13 6 9.1E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		31 38 8 0.13 9 0.12
CUI: C0015310
Disease: Exotropia
Exotropia 		17 21 6 0.12 5 7.7E-02
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		18 32 6 0.12 7 9.5E-02
CUI: C0221358
Disease: Long narrow head
Long narrow head 		19 26 6 0.11 4 5.6E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		39 51 8 0.11 9 9.9E-02
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		30 35 7 0.11 6 7.7E-02
CUI: C0038379
Disease: Strabismus
Strabismus 		61 85 10 0.11 9 7.2E-02
CUI: C0456070
Disease: Growth delay
Growth delay 		31 40 7 0.11 5 6.0E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 69 9 0.11 9 8.3E-02
CUI: C0920299
Disease: Overriding toe
Overriding toe 		13 13 5 0.10 4 6.9E-02
CUI: C0027092
Disease: Myopia
Myopia 		45 52 8 0.10 7 7.4E-02
CUI: C1854882
Disease: Absent speech
Absent speech 		46 72 8 0.10 5 4.3E-02
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		37 39 7 1.0E-01 5 6.0E-02
CUI: C0020490
Disease: Hyperopia
Hyperopia 		16 17 5 9.8E-02 5 8.2E-02
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		16 25 5 9.8E-02 4 5.7E-02
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		128 164 15 9.8E-02 14 7.0E-02
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		39 59 7 9.7E-02 5 4.9E-02
CUI: C1837463
Disease: Narrow face
Narrow face 		6 6 4 9.5E-02 2 3.8E-02
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		18 22 5 9.4E-02 6 9.2E-02
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		19 20 5 9.3E-02 6 9.5E-02
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 37 6 9.1E-02 4 4.9E-02