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: C0033931
Disease: Psychophysiologic Disorders
Psychophysiologic Disorders 		1 0 1 3.6E-02 0 0
CUI: C0277941
Disease: Blanching of skin
Blanching of skin 		1 0 1 3.6E-02 0 0
CUI: C0338900
Disease: Psychasthenic neurosis
Psychasthenic neurosis 		1 0 1 3.6E-02 0 0
CUI: C0542165
Disease: Pseudoparkinsonism
Pseudoparkinsonism 		1 0 1 3.6E-02 0 0
CUI: C0848200
Disease: Afterbirth pain
Afterbirth pain 		1 0 1 3.6E-02 0 0
CUI: C1837154
Disease: Drug Metabolism, Poor, CYP2D6-Related
Drug Metabolism, Poor, CYP2D6-Related 		1 0 1 3.6E-02 0 0
CUI: C3151421
Disease: CYANOSIS, TRANSIENT NEONATAL
CYANOSIS, TRANSIENT NEONATAL 		1 0 1 3.6E-02 0 0
CUI: C3843207
Disease: Sound sensitivity
Sound sensitivity 		1 0 1 3.6E-02 0 0
CUI: C3888911
Disease: CYP2C19 poor metaboliser status
CYP2C19 poor metaboliser status 		1 0 1 3.6E-02 0 0
CUI: C4748197
Disease: OSTEOPETROSIS, AUTOSOMAL DOMINANT 3
OSTEOPETROSIS, AUTOSOMAL DOMINANT 3 		1 0 1 3.6E-02 0 0
CUI: C4749945
Disease: Autism spectrum disorder due to AUTS2 deficiency
Autism spectrum disorder due to AUTS2 deficiency 		1 0 1 3.6E-02 0 0
CUI: C0392477
Disease: Congenital flat foot
Congenital flat foot 		2 0 1 3.4E-02 0 0
CUI: C0472772
Disease: Gamma thalassemia
Gamma thalassemia 		2 0 1 3.4E-02 0 0
CUI: C0859974
Disease: Neonatal intestinal obstruction
Neonatal intestinal obstruction 		2 0 1 3.4E-02 0 0
CUI: C1970197
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7 		2 0 1 3.4E-02 0 0
CUI: C2734068
Disease: Arm span
Arm span 		2 0 1 3.4E-02 0 0
CUI: C4014435
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 26
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 		2 0 1 3.4E-02 0 0
CUI: C4020919
Disease: Dense metaphyseal bands
Dense metaphyseal bands 		2 0 1 3.4E-02 0 0
CUI: C4749023
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70 		2 0 1 3.4E-02 0 0
CUI: C0271995
Disease: HPFH deletion type
HPFH deletion type 		3 0 1 3.3E-02 0 0
CUI: C0392318
Disease: Salivary Gland Infection
Salivary Gland Infection 		3 0 1 3.3E-02 0 0
CUI: C0432261
Disease: Osteopetrosis - intermediate type
Osteopetrosis - intermediate type 		3 0 1 3.3E-02 0 0
CUI: C0456702
Disease: Severe childhood autosomal recessive muscular dystrophy
Severe childhood autosomal recessive muscular dystrophy 		3 0 1 3.3E-02 0 0
CUI: C0521800
Disease: Central cyanosis
Central cyanosis 		3 0 1 3.3E-02 0 0
CUI: C0747078
Disease: Generalized osteopenia
Generalized osteopenia 		3 0 1 3.3E-02 0 0