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: C0266461
Disease: Congenital absence of part of brain
Congenital absence of part of brain 		2 0 2 0.13 0 0
CUI: C0266462
Disease: Congenital hypoplasia of part of brain
Congenital hypoplasia of part of brain 		2 0 2 0.13 0 0
CUI: C0477971
Disease: Other reduction deformities of brain
Other reduction deformities of brain 		2 0 2 0.13 0 0
CUI: C2362742
Disease: Microgyria
Microgyria 		2 0 2 0.13 0 0
CUI: C1879312
Disease: Agyria
Agyria 		20 0 4 0.13 0 0
CUI: C4266441
Disease: Thyroid tumor metastasis
Thyroid tumor metastasis 		3 0 2 0.12 0 0
CUI: C0431375
Disease: Classical Lissencephaly
Classical Lissencephaly 		25 0 4 0.11 0 0
CUI: C3714899
Disease: SYMPHALANGISM, PROXIMAL, 1A
SYMPHALANGISM, PROXIMAL, 1A 		5 0 2 0.11 0 0
CUI: C4054043
Disease: Secondary Peripheral Chondrosarcoma
Secondary Peripheral Chondrosarcoma 		6 0 2 0.11 0 0
CUI: C0333161
Disease: Pseudocyst
Pseudocyst 		8 0 2 9.5E-02 0 0
CUI: C0206641
Disease: Osteochondromatosis
Osteochondromatosis 		10 0 2 8.7E-02 0 0
CUI: C4744565
Disease: Metastatic Colon Carcinoma
Metastatic Colon Carcinoma 		12 0 2 8.0E-02 0 0
CUI: C0266463
Disease: Lissencephaly
Lissencephaly 		71 0 6 7.5E-02 0 0
CUI: C0409345
Disease: Flexion contracture - wrist
Flexion contracture - wrist 		15 0 2 7.1E-02 0 0
CUI: C1840319
Disease: Redundant neck skin
Redundant neck skin 		16 0 2 6.9E-02 0 0
CUI: C0426827
Disease: Gap in ribs
Gap in ribs 		1 0 1 6.7E-02 0 0
CUI: C0580190
Disease: 3-Phosphoglycerate dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency 		1 0 1 6.7E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 6.7E-02 0 0
CUI: C1389473
Disease: Pelvic hypoplasia
Pelvic hypoplasia 		1 0 1 6.7E-02 0 0
CUI: C1844016
Disease: Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence
Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence 		1 0 1 6.7E-02 0 0
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
Lissencephaly, X-Linked, 2 		1 0 1 6.7E-02 0 0
CUI: C1846172
Disease: Hydranencephaly and Abnormal Genitalia
Hydranencephaly and Abnormal Genitalia 		1 0 1 6.7E-02 0 0
CUI: C1850040
Disease: Pelviscapular dysplasia
Pelviscapular dysplasia 		1 0 1 6.7E-02 0 0
CUI: C1850043
Disease: Anterior rounding of vertebral bodies
Anterior rounding of vertebral bodies 		1 0 1 6.7E-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 6.7E-02 0 0