Search results for egr2

32 hits were found for egr2

#	Family	MCID	Name	MIFTS	Score
1	c	CHR653	Charcot-Marie-Tooth Disease, Demyelinating, Type 1d	36	6.132

2		CHR629	Charcot-Marie-Tooth Disease and Deafness	42	6.020

3		NRP060	Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive	50	6.019

4		HYP186	Hypertrophic Neuropathy of Dejerine-Sottas	45	5.869

5	P	CHR071	Charcot-Marie-Tooth Disease	65	5.411

6		TTH006	Tooth Disease	53	4.610

7	P	NRP001	Neuropathy	63	4.307

8	c	CHR113	Charcot-Marie-Tooth Neuropathy Type 1	27	2.873

9		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	56	2.824

10	P	CHR654	Charcot-Marie-Tooth Disease, Axonal, Type 2e	54	2.824

11	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	48	2.824

12	P	CHR625	Charcot-Marie-Tooth Disease, Demyelinating, Type 1b	47	2.824

13		CDQ001	Cauda Equina Syndrome	40	2.824

14	c	CHR646	Charcot-Marie-Tooth Disease, Axonal, Type 2b	39	2.824

15		NRP010	Neuropathy, Hereditary Motor and Sensory, Russe Type	29	2.824

16	c	CHR489	Charcot-Marie-Tooth Disease, Axonal, Type 2q	28	2.824

17		PRP019	Peripheral Nervous System Disease	60	2.112

18		GST053	Gastric Cancer	77	0.136

19		EWN003	Ewing Sarcoma	68	0.111

20		SRC014	Sarcoma	68	0.111

21	P	BPL003	Bipolar Disorder	59	0.111

22	P	HPT023	Hepatocellular Carcinoma	94	0.079

23	c	SYS001	Systemic Lupus Erythematosus	86	0.079

24	P	RTT002	Rett Syndrome	82	0.079

25	P	ATS364	Autism	70	0.079

26	P	SCH015	Schizophrenia	69	0.079

27	P	LPS004	Lupus Erythematosus	68	0.079

28	c	SCL052	Scleroderma, Familial Progressive	64	0.079

29	P	SCL018	Scoliosis	55	0.079

30		PNC041	Pancreatic Ductal Adenocarcinoma	52	0.079

31		ADG002	Audiogenic Seizures	26	0.079

32		CNG102	Congenital Hypomyelination Neuropathy	22	0.079