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: C3279575
Disease: Reticulated skin pigmentation
Reticulated skin pigmentation 		8 0 3 0.14 0 0
CUI: C4721508
Disease: Hamman-Rich Disease
Hamman-Rich Disease 		20 0 4 0.12 0 0
CUI: C2675111
Disease: Abnormal eyelash morphology
Abnormal eyelash morphology 		39 0 6 0.12 0 0
CUI: C0266039
Disease: Taurodontism
Taurodontism 		40 0 6 0.12 0 0
CUI: C1332345
Disease: Atypical Adenomatous Lung Hyperplasia
Atypical Adenomatous Lung Hyperplasia 		2 0 2 0.12 0 0
CUI: C4225356
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6 		2 0 2 0.12 0 0
CUI: C0041974
Disease: Urethral Stenosis
Urethral Stenosis 		41 0 6 0.12 0 0
CUI: C0085660
Disease: Aseptic necrosis
Aseptic necrosis 		41 0 6 0.12 0 0
CUI: C3887513
Disease: Avascular necrosis
Avascular necrosis 		41 0 6 0.12 0 0
CUI: C4531138
Disease: Short telomere length
Short telomere length 		12 0 3 0.12 0 0
CUI: C4553018
Disease: Avascular Necrosis, CTCAE
Avascular Necrosis, CTCAE 		41 0 6 0.12 0 0
CUI: C0034088
Disease: Pulmonary Valve Insufficiency
Pulmonary Valve Insufficiency 		22 0 4 0.11 0 0
CUI: C0423820
Disease: Ridged nails
Ridged nails 		22 0 4 0.11 0 0
CUI: C4024878
Disease: Generalized hyperpigmentation
Generalized hyperpigmentation 		42 0 6 0.11 0 0
CUI: C0034642
Disease: Rales
Rales 		23 0 4 0.11 0 0
CUI: C4721952
Disease: Familial Idiopathic Pulmonary Fibrosis
Familial Idiopathic Pulmonary Fibrosis 		23 0 4 0.11 0 0
CUI: C0232513
Disease: Premature tooth loss
Premature tooth loss 		25 0 4 0.11 0 0
CUI: C0349667
Disease: Sarcoma of breast
Sarcoma of breast 		4 0 2 0.11 0 0
CUI: C2937288
Disease: THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT
THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT 		4 0 2 0.11 0 0
CUI: C3489796
Disease: Thyroid Hormone Resistance, Generalized, Autosomal Recessive
Thyroid Hormone Resistance, Generalized, Autosomal Recessive 		4 0 2 0.11 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation 		59 0 7 0.10 0 0
CUI: C2347751
Disease: Adult Grade I Meningioma
Adult Grade I Meningioma 		6 0 2 9.5E-02 0 0
CUI: C2347760
Disease: Childhood Grade I Meningioma
Childhood Grade I Meningioma 		6 0 2 9.5E-02 0 0
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity 		64 5 7 9.5E-02 1 2.7E-02
CUI: C2931245
Disease: Bone Marrow failure syndromes
Bone Marrow failure syndromes 		41 0 5 9.4E-02 0 0