Search results for Phenelzine

96 hits were found for Phenelzine

#	Family	MCID	Name	MIFTS	Score
1		DPR016	Depression	63	0.349

2		ATY001	Atypical Depressive Disorder	45	0.241

3	P	PNC025	Panic Disorder	53	0.194

4		SCL003	Social Phobia	48	0.178

5		MNT002	Mental Depression	58	0.170

6		SRT004	Serotonin Syndrome	47	0.170

7		END040	Endogenous Depression	55	0.152

8	P	PRS040	Prostate Cancer	97	0.142

9		ANX010	Anxiety	73	0.142

10	P	MJR001	Major Depressive Disorder	68	0.142

11		NRT001	Neurotic Disorder	53	0.142

12		DYS009	Dysthymic Disorder	49	0.142

13		PRT058	Pure Autonomic Failure	59	0.132

14		BRN071	Brain Injury	49	0.120

15		AGR002	Agoraphobia	45	0.120

16	P	HYP263	Hypersomnia	41	0.120

17	P	PRS038	Personality Disorder	65	0.108

18	P	ADN016	Adenocarcinoma	64	0.108

19		BRD004	Borderline Personality Disorder	53	0.108

20		TRM010	Traumatic Brain Injury	51	0.108

21		ATX019	Ataxia with Vitamin E Deficiency	42	0.108

22	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.108

23	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.108

24	P	BRS047	Breast Cancer	97	0.093

25		OBS002	Obsessive-Compulsive Disorder	68	0.093

26	P	TRN020	Turner Syndrome	67	0.093

27		SPN186	Spinal Cord Injury	60	0.093

28	P	PRP019	Peripheral Nervous System Disease	58	0.093

29	P	HDC001	Headache	57	0.093

30	P	NRP001	Neuropathy	56	0.093

31	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.093

32		ALL014	Allergic Encephalomyelitis	38	0.093

33		MLN003	Melancholia	38	0.093

34		PYR016	Pyridoxine Deficiency	30	0.093

35		DWN001	Down Syndrome	70	0.076

36		ALL026	Allergic Hypersensitivity Disease	62	0.076

37		MDD011	Mood Disorder	62	0.076

38	P	ALC033	Alcohol Use Disorder	58	0.076

39		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.076

40		HYP266	Hypoxia	57	0.076

41	P	TRM003	Tremor	54	0.076

42		SXL003	Sexual Disorder	47	0.076

43		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.076

44		MTS001	Mutism	46	0.076

45	P	MYC033	Myoclonus	46	0.076

46		SBC016	Subacute Delirium	44	0.076

47		PYR009	Pyridoxine Deficiency Anemia	34	0.076

48		ELC001	Elective Mutism	23	0.076

49	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.054

50		STR067	Stroke, Ischemic	81	0.054

51	P	SCH015	Schizophrenia	74	0.054

52		CRH001	Crohn's Disease	74	0.054

53		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.054

54	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.054

55		MNT001	Mantle Cell Lymphoma	69	0.054

56		CRB039	Cerebrovascular Disease	67	0.054

57	P	MLG056	Malignant Hyperthermia	67	0.054

58	c	MGR028	Migraine with or Without Aura 1	67	0.054

59		ANG054	Angina Pectoris	66	0.054

60		HYP056	Hypoglycemia	66	0.054

61		ANG020	Angiosarcoma	64	0.054

62	P	NTR004	Neutropenia	63	0.054

63		DRM006	Dermatitis	61	0.054

64		CHR066	Chronic Fatigue Syndrome	61	0.054

65	P	LPS004	Lupus Erythematosus	61	0.054

66		ETN001	Eating Disorder	60	0.054

67	P	MYC008	Myocarditis	59	0.054

68		VSL002	Visual Epilepsy	59	0.054

69		PST028	Post-Traumatic Stress Disorder	58	0.054

70		ISC004	Ischemia	58	0.054

71		FML063	Familial Glucocorticoid Deficiency	58	0.054

72		CNS004	Constipation	58	0.054

73	P	INF032	Infertility	57	0.054

74	c	ACT134	Acute Liver Failure	56	0.054

75	P	SZR006	Seizure Disorder	56	0.054

76		NRL004	Neuroleptic Malignant Syndrome	56	0.054

77	P	DRR001	Diarrhea	55	0.054

78		HMP005	Hemiplegia	55	0.054

79		CLL003	Cellulitis	54	0.054

80		ALC009	Alcoholic Liver Cirrhosis	53	0.054

81		STT041	Stuttering	52	0.054

82		PNG002	Pain Agnosia	51	0.054

83		OCL069	Ocular Motor Apraxia	51	0.054

84		CCN002	Cocaine Abuse	49	0.054

85		47X002	47,xyy	49	0.054

86		QDR001	Quadriplegia	48	0.054

87		PRP007	Priapism	47	0.054

88		ACT084	Acute Stress Disorder	47	0.054

89	c	ACT076	Acute Myocarditis	46	0.054

90		SYN036	Syncope	45	0.054

91	P	MJR007	Major Affective Disorder 1	43	0.054

92		PHB001	Phobic Disorder	41	0.054

93		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.054

94		HND015	Hand Skill, Relative	33	0.054

95		OCC001	Occupational Dermatitis	29	0.054

96		MTR030	Mitral Valve Prolapse, Familial, X-Linked	20	0.054