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: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 2.4E-02 0 0
CUI: C0220692
Disease: Maxillonasal dysplasia, Binder type
Maxillonasal dysplasia, Binder type 		1 0 1 2.4E-02 0 0
CUI: C0234918
Disease: Morbilliform rash
Morbilliform rash 		1 0 1 2.4E-02 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 2.4E-02 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome 		1 0 1 2.4E-02 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus 		1 0 1 2.4E-02 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus 		1 0 1 2.4E-02 0 0
CUI: C0398562
Disease: Triose phosphate isomerase deficiency
Triose phosphate isomerase deficiency 		1 0 1 2.4E-02 0 0
CUI: C0423431
Disease: Subretinal exudate
Subretinal exudate 		1 0 1 2.4E-02 0 0
CUI: C0751679
Disease: Ganglioglioma, Intracranial
Ganglioglioma, Intracranial 		1 0 1 2.4E-02 0 0
CUI: C0795829
Disease: Chromosome 8, trisomy 8q
Chromosome 8, trisomy 8q 		1 0 1 2.4E-02 0 0
CUI: C1275127
Disease: Hyper-IgD periodic fever syndrome (HIDS)
Hyper-IgD periodic fever syndrome (HIDS) 		1 0 1 2.4E-02 0 0
CUI: C1442958
Disease: Actinic porokeratosis
Actinic porokeratosis 		1 0 1 2.4E-02 0 0
CUI: C1834421
Disease: Myxoid subcutaneous tumors
Myxoid subcutaneous tumors 		1 0 1 2.4E-02 0 0
CUI: C1835875
Disease: Normocytic hypoplastic anemia
Normocytic hypoplastic anemia 		1 0 1 2.4E-02 0 0
CUI: C1835881
Disease: Fluctuating hepatomegaly
Fluctuating hepatomegaly 		1 0 1 2.4E-02 0 0
CUI: C1835882
Disease: Fluctuating splenomegaly
Fluctuating splenomegaly 		1 0 1 2.4E-02 0 0
CUI: C1838670
Disease: Myelocytic leukemia-like syndrome, familial, chronic
Myelocytic leukemia-like syndrome, familial, chronic 		1 0 1 2.4E-02 0 0
CUI: C1844579
Disease: Exudative Vitreoretinopathy, Familial, X-Linked Recessive
Exudative Vitreoretinopathy, Familial, X-Linked Recessive 		1 0 1 2.4E-02 0 0
CUI: C1850348
Disease: Hypodysplasia of the corpus callosum
Hypodysplasia of the corpus callosum 		1 0 1 2.4E-02 0 0
CUI: C1850635
Disease: Atrial myxoma, familial
Atrial myxoma, familial 		1 0 1 2.4E-02 0 0
CUI: C1850644
Disease: Anterior bowing of long bones
Anterior bowing of long bones 		1 0 1 2.4E-02 0 0
CUI: C1851430
Disease: Subcortical white matter calcifications
Subcortical white matter calcifications 		1 0 1 2.4E-02 0 0
CUI: C1851431
Disease: Cerebellar calcifications
Cerebellar calcifications 		1 0 1 2.4E-02 0 0
CUI: C1853100
Disease: CEREBROOCULOFACIOSKELETAL SYNDROME 4
CEREBROOCULOFACIOSKELETAL SYNDROME 4 		1 0 1 2.4E-02 0 0