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: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 1 1 5.9E-02 1 8.3E-02
CUI: C0221360
Disease: Congenital absence of diaphragm
Congenital absence of diaphragm 		1 0 1 5.9E-02 0 0
CUI: C0264097
Disease: Calcaneal apophysitis
Calcaneal apophysitis 		1 0 1 5.9E-02 0 0
CUI: C0265756
Disease: Congenital atresia of larynx
Congenital atresia of larynx 		1 0 1 5.9E-02 0 0
CUI: C0431379
Disease: Laminar heterotopia
Laminar heterotopia 		1 0 1 5.9E-02 0 0
CUI: C0580190
Disease: 3-Phosphoglycerate dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency 		1 0 1 5.9E-02 0 0
CUI: C1709573
Disease: Pleural Epithelioid Hemangioendothelioma
Pleural Epithelioid Hemangioendothelioma 		1 0 1 5.9E-02 0 0
CUI: C1835819
Disease: PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)
PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder) 		1 0 1 5.9E-02 0 0
CUI: C1842898
Disease: Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency 		1 0 1 5.9E-02 0 0
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
Lissencephaly and agenesis of corpus callosum 		1 0 1 5.9E-02 0 0
CUI: C1850533
Disease: Yellow subcutaneous tissue covered by thin, scaly skin
Yellow subcutaneous tissue covered by thin, scaly skin 		1 0 1 5.9E-02 0 0
CUI: C1856017
Disease: Adrenal gland dysgenesis
Adrenal gland dysgenesis 		1 0 1 5.9E-02 0 0
CUI: C1856027
Disease: Cleft in skull base
Cleft in skull base 		1 0 1 5.9E-02 0 0
CUI: C1856029
Disease: Proximal tibial hypoplasia
Proximal tibial hypoplasia 		1 0 1 5.9E-02 0 0
CUI: C1857455
Disease: Extension of hair growth on temples to lateral eyebrow
Extension of hair growth on temples to lateral eyebrow 		1 0 1 5.9E-02 0 0
CUI: C1955871
Disease: Cobblestone Complex
Cobblestone Complex 		1 0 1 5.9E-02 0 0
CUI: C2749019
Disease: JOUBERT SYNDROME 10 (disorder)
JOUBERT SYNDROME 10 (disorder) 		1 0 1 5.9E-02 0 0
CUI: C3149907
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13 		1 0 1 5.9E-02 0 0
CUI: C3552528
Disease: Generalized ichthyosis
Generalized ichthyosis 		1 0 1 5.9E-02 0 0
CUI: C3553661
Disease: CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION 		1 0 1 5.9E-02 0 0
CUI: C3553886
Disease: MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 5.9E-02 0 0
CUI: C3806616
Disease: Macular hypopigmented whorls, streaks, and patches
Macular hypopigmented whorls, streaks, and patches 		1 1 1 5.9E-02 1 8.3E-02
CUI: C3810405
Disease: POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE
POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE 		1 0 1 5.9E-02 0 0
CUI: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin 		1 0 1 5.9E-02 0 0
CUI: C4024854
Disease: Irregular hyperpigmentation of back
Irregular hyperpigmentation of back 		1 1 1 5.9E-02 1 8.3E-02