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: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 0.12 0 0
CUI: C0342861
Disease: Uroporphyrinogen decarboxylase deficiency
Uroporphyrinogen decarboxylase deficiency 		1 0 1 0.12 0 0
CUI: C0344987
Disease: Bicuspid pulmonary valve
Bicuspid pulmonary valve 		1 0 1 0.12 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 0.12 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 0 1 0.12 0 0
CUI: C1846422
Disease: Bilobate gallbladder
Bilobate gallbladder 		1 0 1 0.12 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism 		1 0 1 0.12 0 0
CUI: C1867968
Disease: Porphyria Cutanea Tarda, Type I
Porphyria Cutanea Tarda, Type I 		1 0 1 0.12 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 0 1 0.12 0 0
CUI: C2675730
Disease: Deafness, Congenital, and Onychodystrophy, Autosomal Dominant
Deafness, Congenital, and Onychodystrophy, Autosomal Dominant 		1 0 1 0.12 0 0
CUI: C2678486
Disease: Temple-Baraitser Syndrome
Temple-Baraitser Syndrome 		1 0 1 0.12 0 0
CUI: C2678488
Disease: Hypoplasia of terminal phalanges
Hypoplasia of terminal phalanges 		1 0 1 0.12 0 0
CUI: C2931631
Disease: Chromosome 7, trisomy mosaic
Chromosome 7, trisomy mosaic 		1 0 1 0.12 0 0
CUI: C2931707
Disease: Chromosome 15, trisomy mosaicism
Chromosome 15, trisomy mosaicism 		1 0 1 0.12 0 0
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 0 1 0.12 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 0.12 0 0
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		1 0 1 0.12 0 0
CUI: C3552484
Disease: Pseudoepiphysis of the thumb
Pseudoepiphysis of the thumb 		1 0 1 0.12 0 0
CUI: C4020797
Disease: Microtia, second degree
Microtia, second degree 		1 0 1 0.12 0 0
CUI: C4021006
Disease: Short distal phalanx of the 5th toe
Short distal phalanx of the 5th toe 		1 0 1 0.12 0 0
CUI: C4021081
Disease: Absent nail of hallux
Absent nail of hallux 		1 0 1 0.12 0 0
CUI: C4022850
Disease: Hypoplastic thumbnail
Hypoplastic thumbnail 		1 0 1 0.12 0 0
CUI: C4025216
Disease: Prominent nasal septum
Prominent nasal septum 		1 0 1 0.12 0 0