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: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 1 0.11 0 0
CUI: C4021160
Disease: Posterior plagiocephaly
Posterior plagiocephaly 		2 1 1 0.11 1 0.33
CUI: C4022871
Disease: Extra-axial cerebrospinal fluid accumulation
Extra-axial cerebrospinal fluid accumulation 		2 0 1 0.11 0 0
CUI: C4024944
Disease: Profound static encephalopathy
Profound static encephalopathy 		2 0 1 0.11 0 0
CUI: C4225203
Disease: HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2
HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2 		2 14 1 0.11 1 6.2E-02
CUI: C0008519
Disease: Ectopic Tissue
Ectopic Tissue 		3 0 1 1.0E-01 0 0
CUI: C0037952
Disease: Spinocerebellar Degeneration
Spinocerebellar Degeneration 		14 0 2 1.0E-01 0 0
CUI: C0039234
Disease: Tachycardia, Ectopic Atrial
Tachycardia, Ectopic Atrial 		3 0 1 1.0E-01 0 0
CUI: C0153886
Disease: Acute myeloid leukemia in remission
Acute myeloid leukemia in remission 		3 0 1 1.0E-01 0 0
CUI: C0523957
Disease: Tryptophan measurement
Tryptophan measurement 		3 0 1 1.0E-01 0 0
CUI: C1519714
Disease: Type II Endometrial Adenocarcinoma
Type II Endometrial Adenocarcinoma 		3 0 1 1.0E-01 0 0
CUI: C1846386
Disease: Focal Cortical Dysplasia of Taylor, Type IIa
Focal Cortical Dysplasia of Taylor, Type IIa 		3 0 1 1.0E-01 0 0
CUI: C1846389
Disease: Focal Cortical Dysplasia of Taylor, Type IIb
Focal Cortical Dysplasia of Taylor, Type IIb 		3 0 1 1.0E-01 0 0
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 0 1 1.0E-01 0 0
CUI: C1860606
Disease: Short proximal phalanx of finger
Short proximal phalanx of finger 		3 0 1 1.0E-01 0 0
CUI: C2853920
Disease: Lymphoblastic T-cell lymphoma
Lymphoblastic T-cell lymphoma 		3 0 1 1.0E-01 0 0
CUI: C2931355
Disease: Spastic paraplegia 3, autosomal dominant
Spastic paraplegia 3, autosomal dominant 		3 0 1 1.0E-01 0 0
CUI: C4324689
Disease: Pauci-immune glomerulonephritis
Pauci-immune glomerulonephritis 		3 0 1 1.0E-01 0 0
CUI: C4476710
Disease: Delayed ability to sit
Delayed ability to sit 		3 0 1 1.0E-01 0 0
CUI: C4551850
Disease: Eyelid myoclonias
Eyelid myoclonias 		3 0 1 1.0E-01 0 0
CUI: C0268494
Disease: Oculocutaneous albinism type 1
Oculocutaneous albinism type 1 		4 0 1 9.1E-02 0 0
CUI: C1335996
Disease: Gastrointestinal stromal tumor of small intestine
Gastrointestinal stromal tumor of small intestine 		4 0 1 9.1E-02 0 0
CUI: C3278658
Disease: Linear hyperpigmentation
Linear hyperpigmentation 		4 0 1 9.1E-02 0 0
CUI: C3532947
Disease: Severe receptive language delay
Severe receptive language delay 		4 0 1 9.1E-02 0 0
CUI: C4022575
Disease: Inertia
Inertia 		4 0 1 9.1E-02 0 0