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: C0201512
Disease: Thyroglobulin antibody measurement
Thyroglobulin antibody measurement 		10 0 1 1.4E-04 0 0
CUI: C0202159
Disease: Parathyroid hormone measurement
Parathyroid hormone measurement 		10 0 1 1.4E-04 0 0
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1 		10 0 1 1.4E-04 0 0
CUI: C3552099
Disease: Respiratory insufficiency due to defective ciliary clearance
Respiratory insufficiency due to defective ciliary clearance 		10 0 1 1.4E-04 0 0
CUI: C0271092
Disease: Progressive cone dystrophy (without rod involvement)
Progressive cone dystrophy (without rod involvement) 		9 0 1 1.4E-04 0 0
CUI: C1848595
Disease: Mesoaxial polydactyly
Mesoaxial polydactyly 		9 0 1 1.4E-04 0 0
CUI: C1848597
Disease: Central Y-shaped metacarpal
Central Y-shaped metacarpal 		9 0 1 1.4E-04 0 0
CUI: C1856655
Disease: Hypoplasia of olfactory tract
Hypoplasia of olfactory tract 		9 0 1 1.4E-04 0 0
CUI: C2732374
Disease: Edema of dorsum of hand
Edema of dorsum of hand 		9 0 1 1.4E-04 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies 		9 0 1 1.4E-04 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 1 1.4E-04 0 0
CUI: C0268540
Disease: HHH syndrome
HHH syndrome 		8 0 1 1.4E-04 0 0
CUI: C0268594
Disease: Glutaric aciduria
Glutaric aciduria 		8 0 1 1.4E-04 0 0
CUI: C1306122
Disease: Oguchi disease
Oguchi disease 		8 0 1 1.4E-04 0 0
CUI: C1695776
Disease: Vertebral wedging
Vertebral wedging 		8 0 1 1.4E-04 0 0
CUI: C4021581
Disease: Distal upper limb amyotrophy
Distal upper limb amyotrophy 		8 0 1 1.4E-04 0 0
CUI: C4022586
Disease: Fatigable weakness of skeletal muscles
Fatigable weakness of skeletal muscles 		8 0 1 1.4E-04 0 0
CUI: C0005833
Disease: Blood Sedimentation
Blood Sedimentation 		7 0 1 1.4E-04 0 0
CUI: C0017927
Disease: Glycogen Storage Disease Type VIII
Glycogen Storage Disease Type VIII 		7 0 1 1.4E-04 0 0
CUI: C0175692
Disease: Johanson-Blizzard syndrome
Johanson-Blizzard syndrome 		7 0 1 1.4E-04 0 0
CUI: C0234398
Disease: Visual Cortex Disorder
Visual Cortex Disorder 		7 0 1 1.4E-04 0 0
CUI: C1291564
Disease: Deficiency of aromatic-L-amino-acid decarboxylase
Deficiency of aromatic-L-amino-acid decarboxylase 		7 0 1 1.4E-04 0 0
CUI: C1332140
Disease: Acrofacial Dysostosis
Acrofacial Dysostosis 		7 0 1 1.4E-04 0 0
CUI: C1836876
Disease: Pierson syndrome
Pierson syndrome 		7 0 1 1.4E-04 0 0
CUI: C1848556
Disease: Decreased adenosylcobalamin
Decreased adenosylcobalamin 		7 0 1 1.4E-04 0 0