Search results for Chloral hydrate

114 hits were found for Chloral hydrate

#	Family	MCID	Name	MIFTS	Score
1		TTN003	Tetanus	65	0.212

2		CHL014	Cholera	59	0.192

3		SBC016	Subacute Delirium	44	0.188

4	P	DRR001	Diarrhea	55	0.187

5	P	CTR002	Cataract	60	0.175

6		48X005	48,xyyy	39	0.168

7	P	SZR006	Seizure Disorder	56	0.163

8		CRD223	Cardiac Arrhythmia	60	0.142

9		PNG002	Pain Agnosia	51	0.141

10	P	HRT032	Heart Disease	75	0.140

11	P	EPL164	Epilepsy	71	0.137

12	P	EXN002	Exanthem	57	0.137

13		ATX019	Ataxia with Vitamin E Deficiency	42	0.137

14	P	ENC018	Encephalopathy	61	0.136

15		HYP266	Hypoxia	57	0.134

16		PRT036	Peritonitis	64	0.127

17		VSL002	Visual Epilepsy	59	0.127

18		BRN002	Bronchiolitis	59	0.124

19		RFR003	Refractive Error	43	0.124

20		ILS001	Ileus	51	0.122

21	P	DMN002	Dementia	66	0.118

22		AYM001	Ayme-Gripp Syndrome	57	0.115

23		DYS073	Dysphagia	50	0.114

24		ANX010	Anxiety	73	0.113

25	P	ATS364	Autism	70	0.111

26		MTH071	Methane Production	26	0.106

27		OCL069	Ocular Motor Apraxia	51	0.104

28	c	DRR009	Diarrhea 6	46	0.104

29		CNS004	Constipation	58	0.103

30		PLM010	Pulmonary Edema	54	0.103

31		CRB037	Cerebral Palsy	69	0.102

32		47X002	47,xyy	49	0.101

33		ALL026	Allergic Hypersensitivity Disease	62	0.098

34	P	SLP006	Sleep Apnea	69	0.098

35		DFC004	Deficiency Anemia	70	0.095

36	P	ECL001	Eclampsia	50	0.095

37		PPL049	Papillon-Lefevre Syndrome	65	0.093

38		SPS003	Spastic Diplegia	51	0.093

39		NND010	Nondisjunction	34	0.093

40		GST045	Gastroenteritis	59	0.093

41	P	TRM003	Tremor	54	0.093

42		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.091

43		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.091

44		ANX004	Anoxia	40	0.091

45	P	MYC033	Myoclonus	46	0.090

46	P	RSP003	Respiratory Failure	74	0.087

47		KHL003	Kohlschutter-Tonz Syndrome	65	0.086

48		CRB004	Cerebral Artery Occlusion	45	0.086

49		LNG099	Lung Disease	60	0.083

50		STT001	Status Epilepticus	60	0.082

51		TRM010	Traumatic Brain Injury	51	0.082

52		BRN071	Brain Injury	49	0.082

53		CHL079	Children's Interstitial Lung Disease	26	0.082

54		NWB001	Newborn Respiratory Distress Syndrome	58	0.080

55		BRN004	Brain Edema	56	0.080

56		DWN001	Down Syndrome	70	0.076

57		LYM019	Lymphosarcoma	46	0.076

58	P	SCH015	Schizophrenia	74	0.076

59	P	CRD119	Cardiac Arrest	67	0.076

60	P	ERL057	Early Infantile Epileptic Encephalopathy	63	0.076

61		DPR016	Depression	63	0.076

62		MNT002	Mental Depression	58	0.076

63		HMP005	Hemiplegia	55	0.076

64	P	ALT001	Alternating Hemiplegia of Childhood	53	0.076

65		SMT006	Somatoform Disorder	50	0.076

66		AMB002	Amblyopia	49	0.076

67		SMT001	Somatization Disorder	46	0.076

68		SPP007	Suppression Amblyopia	39	0.076

69	c	ALC016	Alcohol Sensitivity, Acute	31	0.076

70		OHT001	Ohtahara Syndrome	21	0.076

71	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.067

72	c	ACT073	Acute Leukemia	58	0.067

73		BLR008	Bilirubin Metabolic Disorder	57	0.067

74		AST005	Asthma	76	0.061

75	P	CNR004	Cone-Rod Dystrophy 2	73	0.061

76		ATH013	Atherosclerosis Susceptibility	65	0.061

77	P	ESP024	Esophagitis	62	0.061

78		PRP030	Purpura	54	0.061

79	P	FBR031	Febrile Seizures	53	0.061

80	P	DDN001	Duodenal Ulcer	52	0.061

81		HDN002	Head Injury	46	0.061

82		CYT002	Cytokine Deficiency	42	0.061

83	P	NRB001	Neuroblastoma	72	0.054

84		LGH007	Leigh Syndrome	70	0.054

85		PLM001	Pulmonary Tuberculosis	69	0.054

86		SKN019	Skin Melanoma	68	0.054

87	P	HYP098	Hypereosinophilic Syndrome	67	0.054

88	P	PLM037	Pulmonary Hypertension	67	0.054

89	P	HYD006	Hydrocephalus	66	0.054

90		KRN002	Kearns-Sayre Syndrome	63	0.054

91	P	KDN017	Kidney Cancer	60	0.054

92		ING001	Inguinal Hernia	60	0.054

93		ADN018	Adenoma	59	0.054

94		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.054

95	P	TYR004	Tyrosinemia	58	0.054

96		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.054

97	P	MYS005	Myositis	56	0.054

98		END040	Endogenous Depression	55	0.054

99		PRS045	Prostatic Hypertrophy	53	0.054

100		EXP004	Exophthalmos	52	0.054

101		DRG003	Drug Dependence	47	0.054

102	c	CNG216	Congenital Hydrocephalus	47	0.054

103	c	CHR095	Chronic Progressive External Ophthalmoplegia	46	0.054

104		EPD015	Epidemic Typhus	45	0.054

105		CYN002	Cyanosis, Transient Neonatal	45	0.054

106		HPT067	Hepatocellular Adenoma	44	0.054

107		CRP002	Croup	44	0.054

108	c	PRG011	Progressive Myoclonus Epilepsy	42	0.054

109		NNT008	Neonatal Abstinence Syndrome	41	0.054

110		PLY100	Polyploidy	40	0.054

111	P	FML340	Familial Episodic Pain Syndrome	39	0.054

112		FST001	Foster-Kennedy Syndrome	36	0.054

113		CHR178	Chromosomal Triplication	35	0.054

114	P	MYC026	Myoclonus Epilepsy	35	0.054