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: C0040947
Disease: Trichostrongyloidiasis
Trichostrongyloidiasis 		1 0 1 1.00 0 0
CUI: C1334180
Disease: Inflammatory malignant fibrous histiocytoma
Inflammatory malignant fibrous histiocytoma 		1 0 1 1.00 0 0
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		1 0 1 1.00 0 0
CUI: C0852418
Disease: Speech and language abnormalities
Speech and language abnormalities 		2 0 1 0.50 0 0
CUI: C1862177
Disease: Diaphyseal medullary stenosis with malignant fibrous histiocytoma
Diaphyseal medullary stenosis with malignant fibrous histiocytoma 		2 0 1 0.50 0 0
CUI: C4023518
Disease: Abnormality of skin adnexa morphology
Abnormality of skin adnexa morphology 		2 2 1 0.50 1 4.3E-02
CUI: C0003564
Disease: Aphonia
Aphonia 		4 0 1 0.25 0 0
CUI: C0796095
Disease: Opitz trigonocephaly syndrome
Opitz trigonocephaly syndrome 		4 0 1 0.25 0 0
CUI: C1851897
Disease: Anterior creases of earlobe
Anterior creases of earlobe 		4 0 1 0.25 0 0
CUI: C0155922
Disease: Tooth development and eruption disorder
Tooth development and eruption disorder 		5 0 1 0.20 0 0
CUI: C1335060
Disease: Non-Small Cell Adenocarcinoma
Non-Small Cell Adenocarcinoma 		5 0 1 0.20 0 0
CUI: C1857278
Disease: Partial or complete agenesis of corpus callosum
Partial or complete agenesis of corpus callosum 		5 6 1 0.20 1 3.7E-02
CUI: C1970117
Disease: Tooth Agenesis, Selective, With Orofacial Cleft
Tooth Agenesis, Selective, With Orofacial Cleft 		5 0 1 0.20 0 0
CUI: C1970118
Disease: Hypodontia Oligodontia with Orofacial Cleft
Hypodontia Oligodontia with Orofacial Cleft 		5 0 1 0.20 0 0
CUI: C1854408
Disease: Glabellar hemangioma
Glabellar hemangioma 		6 0 1 0.17 0 0
CUI: C3805727
Disease: MEGALENCEPHALY, AUTOSOMAL DOMINANT
MEGALENCEPHALY, AUTOSOMAL DOMINANT 		6 5 1 0.17 1 3.8E-02
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
TOOTH AGENESIS, SELECTIVE, 9 		6 0 1 0.17 0 0
CUI: C4479708
Disease: FCD IIA
FCD IIA 		6 0 1 0.17 0 0
CUI: C1335483
Disease: Gastric Diffuse Large B-Cell Lymphoma
Gastric Diffuse Large B-Cell Lymphoma 		8 0 1 0.12 0 0
CUI: C3828492
Disease: Pre-Gestational Diabetes
Pre-Gestational Diabetes 		8 0 1 0.12 0 0
CUI: C1185616
Disease: Hair whorls
Hair whorls 		9 5 1 0.11 1 3.8E-02
CUI: C1833736
Disease: Osteogenesis imperfecta, Levin type
Osteogenesis imperfecta, Levin type 		9 0 1 0.11 0 0
CUI: C2698750
Disease: Pediatric follicular lymphoma
Pediatric follicular lymphoma 		10 0 1 1.0E-01 0 0
CUI: C3489529
Disease: Tooth Agenesis, Familial
Tooth Agenesis, Familial 		10 0 1 1.0E-01 0 0
CUI: C0023009
Disease: Speech and language disorder
Speech and language disorder 		11 0 1 9.1E-02 0 0