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: C0020449
Disease: Hyperdistention
Hyperdistention
0 1 0 0 1 3.9E-03
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0 67 0 0 1 3.1E-03
CUI: C4744444
Disease: Metastatic Lung Adenocarcinoma
Metastatic Lung Adenocarcinoma
0 10 0 0 1 3.7E-03
CUI: C0263429
Disease: Atrophoderma vermiculatum
Atrophoderma vermiculatum
1 0 1 2.4E-02 0 0
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
Benign Lymphoproliferative Disorder
1 0 1 2.4E-02 0 0
CUI: C1334682
Disease: Mediastinal teratoma
Mediastinal teratoma
1 0 1 2.4E-02 0 0
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
1 0 1 2.4E-02 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor
1 0 1 2.4E-02 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome
1 0 1 2.4E-02 0 0
Fusion of the left and right thalami
1 0 1 2.4E-02 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7
1 0 1 2.4E-02 0 0
Anomalous branches of internal carotid artery
1 0 1 2.4E-02 0 0
CUI: C1857946
Disease: Severe gastroesophageal reflux
Severe gastroesophageal reflux
1 0 1 2.4E-02 0 0
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
1 0 1 2.4E-02 0 0
Bacteremia caused by Gram-negative bacteria
1 0 1 2.4E-02 0 0
CUI: C3711390
Disease: 9q22.3 Microdeletion
9q22.3 Microdeletion
1 0 1 2.4E-02 0 0
CUI: C3805371
Disease: Pits of palms and soles
Pits of palms and soles
1 0 1 2.4E-02 0 0
CUI: C3808786
Disease: ALBINISM, OCULOCUTANEOUS, TYPE VII
ALBINISM, OCULOCUTANEOUS, TYPE VII
1 0 1 2.4E-02 0 0
CUI: C3809803
Disease: MICROPHTHALMIA, SYNDROMIC 12
MICROPHTHALMIA, SYNDROMIC 12
1 0 1 2.4E-02 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
1 0 1 2.4E-02 0 0
Enlarged epiphyses of the proximal phalanges of the hand
1 0 1 2.4E-02 0 0
Contracture of the distal interphalangeal joint of the fingers
1 0 1 2.4E-02 0 0
CUI: C4025542
Disease: Humeral cortical thickening
Humeral cortical thickening
1 0 1 2.4E-02 0 0
CUI: C4025842
Disease: Abnormal uvea morphology
Abnormal uvea morphology
1 0 1 2.4E-02 0 0
RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2
1 0 1 2.4E-02 0 0