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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 4.3E-02 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 4.3E-02 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 4.3E-02 0 0
CUI: C0265729
Disease: Mesatipellic pelvis
Mesatipellic pelvis 		1 0 1 4.3E-02 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth 		1 0 1 4.3E-02 0 0
CUI: C0272282
Disease: Thrombocytopenia, cyclic
Thrombocytopenia, cyclic 		1 0 1 4.3E-02 0 0
CUI: C0339965
Disease: Hemorrhagic pneumonia
Hemorrhagic pneumonia 		1 0 1 4.3E-02 0 0
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
Gorlin Chaudhry Moss syndrome 		1 0 1 4.3E-02 0 0
CUI: C0686761
Disease: Lack of bone formation
Lack of bone formation 		1 0 1 4.3E-02 0 0
CUI: C0694457
Disease: Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) 		1 0 1 4.3E-02 0 0
CUI: C0743924
Disease: Short fetal femur length
Short fetal femur length 		1 0 1 4.3E-02 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome 		1 0 1 4.3E-02 0 0
CUI: C0795932
Disease: fontaine syndrome
fontaine syndrome 		1 0 1 4.3E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 4.3E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 4.3E-02 0 0
CUI: C1334963
Disease: Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma
Nevoid Basal Cell Carcinoma Syndrome Associated Medulloblastoma 		1 0 1 4.3E-02 0 0
CUI: C1368295
Disease: Malignant basal cell tumor
Malignant basal cell tumor 		1 0 1 4.3E-02 0 0
CUI: C1834038
Disease: Schilbach-Rott Syndrome
Schilbach-Rott Syndrome 		1 0 1 4.3E-02 0 0
CUI: C1834930
Disease: Fusion of the left and right thalami
Fusion of the left and right thalami 		1 0 1 4.3E-02 0 0
CUI: C1834969
Disease: Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly
Metaphyseal Dysplasia with Maxillary Hypoplasia and Brachydactyly 		1 0 1 4.3E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 4.3E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 4.3E-02 0 0
CUI: C1835602
Disease: Aplastic/hypoplastic lacrimal glands
Aplastic/hypoplastic lacrimal glands 		1 0 1 4.3E-02 0 0
CUI: C1835820
Disease: HOLOPROSENCEPHALY 7
HOLOPROSENCEPHALY 7 		1 0 1 4.3E-02 0 0
CUI: C1837756
Disease: MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY 		1 0 1 4.3E-02 0 0