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: C0268323
Disease: Familial porphyria cutanea tarda
Familial porphyria cutanea tarda 		2 0 2 0.25 0 0
CUI: C4551773
Disease: ZIMMERMANN-LABAND SYNDROME 1
ZIMMERMANN-LABAND SYNDROME 1 		2 0 2 0.25 0 0
CUI: C3805877
Disease: Hyperpigmentation in sun-exposed areas
Hyperpigmentation in sun-exposed areas 		3 0 2 0.22 0 0
CUI: C4025825
Disease: Abnormal external genitalia
Abnormal external genitalia 		3 0 2 0.22 0 0
CUI: C1276127
Disease: Sporadic porphyria cutanea tarda
Sporadic porphyria cutanea tarda 		4 0 2 0.20 0 0
CUI: C1848769
Disease: Overtubulated long bones
Overtubulated long bones 		4 0 2 0.20 0 0
CUI: C3277940
Disease: Generalized hypertrichosis
Generalized hypertrichosis 		6 0 2 0.17 0 0
CUI: C4024168
Disease: Thickened ears
Thickened ears 		7 0 2 0.15 0 0
CUI: C0796013
Disease: Zimmerman Laband syndrome
Zimmerman Laband syndrome 		8 0 2 0.14 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 2 0.14 0 0
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