Term	es	nes	pval	sidak	fdr	geneset_size	leading_edge	leading_edge_size
Alzheimer disease	0.9418182063053556	2.058432321216473	0.0395486517711933	0.9903468821192812	0.4334893877341303	4	P49840	1
Diabetes mellitus	0.7371108747430651	1.977394043420188	0.0479971067576612	0.9965053728279764	0.4334893877341303	9	P49840,P49841	2
Dwarfism	0.5055328691228714	1.835741039715779	0.0663959652013543	0.9996295643340136	0.5090357332103835	43	O75718,O95831,Q32P28,Q96HY6,Q14739,Q96PZ0	6
Amyotrophic lateral sclerosis	0.6063676054926043	1.7410265676593473	0.0816789216702229	0.9999444896996827	0.5760428659631595	13	Q99720,P50995,Q96CV9,P35637	4
Leber hereditary optic neuropathy	0.9676998368678612	1.58845311141903	0.1121839157522854	0.9999988593668148	0.5930792912473026	2	P00846	1
Zellweger syndrome	0.8117415252298816	1.5606097442278974	0.1186158582494605	0.9999995056873712	0.5930792912473026	4	O75381	1
Peroxisome biogenesis disorder	0.8117415252298816	1.5606097442278974	0.1186158582494605	0.9999995056873712	0.5930792912473026	4	O75381	1
Retinitis pigmentosa	0.5186842919868717	1.258906068814495	0.2080642615375569	0.9999999999977648	0.8599628160453194	13	O75695,P00846	2
Osteogenesis imperfecta	0.5634124289232968	1.1619044040180726	0.2452742980326723	0.9999999999999912	0.8599628160453194	9	Q32P28,O75718,P07237	3
Hirschsprung disease	0.8541598694942805	1.140135299502963	0.2542299375917629	0.9999999999999978	0.8599628160453194	2	P42892	1
Charcot-Marie-Tooth disease	0.4060711639386145	0.9442500916159372	0.3450418631807341	1.0	0.8599628160453194	24	P54802,O95831	2
Congenital disorder of glycosylation	0.4368074295377537	0.9317551768732693	0.3514630639489566	1.0	0.8599628160453194	17	Q8TCJ2,Q8N511	2
Glaucoma	0.7738874794721082	0.8146665347595019	0.4152632140767858	1.0	0.925885483196342	3	Q96CV9	1
Ehlers-Danlos syndrome	0.7673735725937858	0.8100703080439218	0.417899768203779	1.0	0.925885483196342	2	Q9NWM8	1
Deafness	0.3710930825848577	0.7740620707261815	0.4388940859588377	1.0	0.925885483196342	47	Q13217,Q15067,Q9NR28,O95831,Q96GW9,Q16740,Q9NWM8	7
Dystroglycanopathy	0.5441795629878207	0.7594749746733117	0.4475684786464042	1.0	0.925885483196342	5	Q8NAT1	1
Primary mitochondrial disease	0.3470127280194635	0.71588613773048	0.474061658698139	1.0	0.925885483196342	98	O95831,Q99797,Q6DKK2,P14927,P00846,Q9HA77,Q96GW9,Q9Y606,Q9BQT8,P22695,Q8NI60,P39210,Q5ST30,Q5U5X0,P03915,Q9Y584,Q8N183,Q70HW3,O00217,P08574,P00403,O43676	22
Leigh syndrome	0.4402643183267091	0.6958604547181101	0.4865162247728785	1.0	0.925885483196342	11	P00846	1
Allergen	0.7318107667210425	0.682547524864601	0.4948928023971239	1.0	0.925885483196342	2	O43290	1
Emery-Dreifuss muscular dystrophy	0.5205946223748064	0.6669163701465374	0.5048255538163113	1.0	0.925885483196342	5	Q9BTV4,P50402,Q8WXH0	3
Congenital muscular dystrophy	0.4921396174675604	0.647173690814959	0.5175195366405447	1.0	0.925885483196342	6	O60762,Q8NAT1,P02545	3
Limb-girdle muscular dystrophy	0.4353389034233462	0.5656513710011353	0.5716307988770006	1.0	0.925885483196342	9	O14979,Q15149,Q5JTV8,P02545,Q8NAT1	5
Proto-oncogene	0.3459708432260865	0.5340704610240571	0.5932927857096015	1.0	0.925885483196342	44	Q06136,P07948,Q03164,P12270,Q16204,Q92804,P17252,P35637,Q96T37,Q01105	10
Dystonia	0.4422488510140901	0.533121760052469	0.5939492969835902	1.0	0.925885483196342	7	P11166,O75569,Q15043,P35270	4
Schizophrenia	0.6810703575143497	0.5188886994691034	0.6038383586063101	1.0	0.925885483196342	3	Q9NTZ6	1
Neuropathy	0.3335983005179828	0.4771153759120379	0.6332799662669979	1.0	0.9357202128670054	48	Q13217,P00846,Q15067,O95831,P54802	5
Lissencephaly	0.3950540302900354	0.4366791668954281	0.6623440399470679	1.0	0.9429706879522	10	Q8NAT1,O00139,P07942,Q9Y320	4
Glutaricaciduria	0.4779627815866669	0.3380096248964944	0.7353559346106919	1.0	0.9825617494502108	4	P38117,Q16134,Q92947	3
Gaucher disease	0.5797716150081446	0.2427565064409127	0.8081940306181483	1.0	1.0	2	P07602	1
Ciliopathy	0.3510149612944748	0.2204467258476647	0.8255232583624963	1.0	1.0	8	P49454,P49959	2
Rhizomelic chondrodysplasia punctata	0.4792822185970516	0.0913756684385874	0.9271940946275136	1.0	1.0	2	O00116	1
Cockayne syndrome	0.476998368678618	0.0892939280748463	0.9288483194891644	1.0	1.0	2	P19447	1
Fanconi anemia	0.4407830342577444	0.0630109093375809	0.9497578171903522	1.0	1.0	2	Q9NVI1	1
Alport syndrome	0.4388254486133703	0.0619196299935364	0.9506268350178984	1.0	1.0	2	P35579	1
Hereditary nonpolyposis colorectal cancer	0.4146818923327835	0.0508042206256163	0.9594815276495254	1.0	1.0	2	P52701	1
Systemic lupus erythematosus	0.3234334203655425	0.0265808085056827	0.9787940804452702	1.0	1.0	3	P05455,P12956	2