Source: ALL
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: C1837142
Disease: Poor suck
Poor suck 		103 0 39 0.25 0 0
CUI: C0042454
Disease: Velopharyngeal Insufficiency
Velopharyngeal Insufficiency 		27 0 18 0.18 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		165 0 34 0.15 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 34 0.15 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 35 0.15 0 0
CUI: C1857632
Disease: Narrow palm
Narrow palm 		17 0 14 0.15 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 36 0.14 0 0
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME 		18 0 13 0.13 0 0
CUI: C1858025
Disease: Spinal rigidity
Spinal rigidity 		55 0 17 0.13 0 0
CUI: C0265222
Disease: Royer Syndrome
Royer Syndrome 		12 0 12 0.13 0 0
CUI: C1386091
Disease: Acromicria
Acromicria 		13 0 12 0.13 0 0
CUI: C0556280
Disease: Gross motor impairment
Gross motor impairment 		22 0 13 0.13 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 16 0.13 0 0
CUI: C0232608
Disease: Nasal regurgitation
Nasal regurgitation 		14 0 12 0.13 0 0
CUI: C1849923
Disease: Generalized hypopigmentation
Generalized hypopigmentation 		23 0 13 0.13 0 0
CUI: C1865313
Disease: Speech articulation difficulties
Speech articulation difficulties 		23 0 13 0.13 0 0
CUI: C3203358
Disease: Hypoventilation
Hypoventilation 		28 0 13 0.12 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum 		57 0 16 0.12 0 0
CUI: C0265287
Disease: Acromicric Dysplasia
Acromicric Dysplasia 		21 0 12 0.12 0 0
CUI: C0311277
Disease: Obesity, Abdominal
Obesity, Abdominal 		21 0 12 0.12 0 0
CUI: C1837522
Disease: Impaired pain sensation
Impaired pain sensation 		41 0 14 0.12 0 0
CUI: C3807025
Disease: Intermittent episodes of respiratory insufficiency due to muscle weakness
Intermittent episodes of respiratory insufficiency due to muscle weakness 		14 0 11 0.11 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 14 0.11 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge 		47 0 14 0.11 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 0 14 0.11 0 0