Search results for egr2

69 hits were found for egr2

#	Family	MCID	Name	MIFTS	Score
1	P	NRP063	Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive	57	5.817

2	c	CHR653	Charcot-Marie-Tooth Disease, Demyelinating, Type 1d	40	5.487

3	P	CHR071	Charcot-Marie-Tooth Disease	65	5.473

4		HYP186	Hypertrophic Neuropathy of Dejerine-Sottas	51	4.899

5		CHR629	Charcot-Marie-Tooth Disease and Deafness	52	4.492

6		TTH006	Tooth Disease	46	4.169

7		CHR687	Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy	41	3.852

8	P	NRP001	Neuropathy	56	3.819

9	P	SCL018	Scoliosis	60	2.537

10	P	PLY019	Polyneuropathy	56	2.537

11	P	RTT002	Rett Syndrome	80	2.502

12		SNS003	Sensory Peripheral Neuropathy	54	2.502

13	P	CHR654	Charcot-Marie-Tooth Disease, Axonal, Type 2e	59	2.461

14	P	PRP019	Peripheral Nervous System Disease	58	1.956

15	P	CHR640	Charcot-Marie-Tooth Disease, X-Linked Dominant, 1	56	1.836

16		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	59	1.794

17	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	55	1.794

18		NRP010	Neuropathy, Hereditary Motor and Sensory, Russe Type	36	1.794

19		CNT097	Central Hypoventilation Syndrome, Congenital	71	1.740

20		NRM005	Neuromuscular Disease	64	1.740

21	P	CHR625	Charcot-Marie-Tooth Disease, Demyelinating, Type 1b	57	1.740

22		PRP066	Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease	51	1.740

23	c	CHR647	Charcot-Marie-Tooth Disease, Demyelinating, Type 1c	46	1.740

24	c	CHR376	Charcot-Marie-Tooth Disease, Type 4d	46	1.740

25	c	CHR517	Charcot-Marie-Tooth Disease, Type 4a	45	1.740

26		PLX002	Plexiform Neurofibroma	44	1.740

27	c	CHR670	Charcot-Marie-Tooth Disease, Demyelinating, Type 4f	43	1.740

28	c	CHR657	Charcot-Marie-Tooth Disease, Axonal, Type 2j	39	1.740

29	c	CHR641	Charcot-Marie-Tooth Disease, X-Linked Recessive, 2	34	1.740

30	P	PPL023	Pupil Disease	28	1.740

31	c	CHR026	Charcot-Marie-Tooth Disease Type X	25	1.740

32		ARG003	Argyll Robertson Pupil	22	1.740

33		ABN004	Abnormal Pupillary Function	15	1.740

34		ATM095	Autoimmune Disease	62	0.161

35		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.131

36	P	GST053	Gastric Cancer	83	0.114

37		EWN003	Ewing Sarcoma	69	0.093

38		SRC014	Sarcoma	65	0.093

39	P	BPL003	Bipolar Disorder	56	0.093

40		SPN035	Spindle Cell Sarcoma	53	0.093

41	c	MJR024	Major Affective Disorder 9	41	0.093

42	c	MJR022	Major Affective Disorder 8	38	0.093

43	c	HRD088	Hereditary Neuropathies	37	0.093

44	c	SYS001	Systemic Lupus Erythematosus	86	0.066

45	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.066

46	P	SCH015	Schizophrenia	74	0.066

47	P	NRB001	Neuroblastoma	72	0.066

48	P	PHC003	Pheochromocytoma	71	0.066

49	P	ATS364	Autism	70	0.066

50	P	SYS005	Systemic Scleroderma	68	0.066

51	P	INF038	Influenza	68	0.066

52	P	MTR014	Motor Neuron Disease	65	0.066

53	c	SCL052	Scleroderma, Familial Progressive	61	0.066

54	P	LPS004	Lupus Erythematosus	61	0.066

55		THY029	Thyroid Carcinoma	59	0.066

56		VSL002	Visual Epilepsy	59	0.066

57	P	SZR006	Seizure Disorder	56	0.066

58	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.066

59	P	TRM003	Tremor	54	0.066

60		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.066

61	c	CHR516	Charcot-Marie-Tooth Disease, Type 4c	50	0.066

62		HLX001	Helix Syndrome	47	0.066

63		ADR040	Adrenal Gland Pheochromocytoma	46	0.066

64		CRB004	Cerebral Artery Occlusion	45	0.066

65	P	DMY001	Demyelinating Polyneuropathy	43	0.066

66		SYS071	Systemic Autoimmune Disease	37	0.066

67	P	AXN001	Axonal Neuropathy	36	0.066

68		ADG002	Audiogenic Seizures	25	0.066

69		GJB007	Gjb1 Disorders: Charcot Marie Tooth Neuropathy and Central Nervous System Phenotypes	8	0.066