Search results for acid-labile subunit

66 hits were found for acid-labile subunit

#	Family	MCID	Name	MIFTS	Score
1		ACD008	Acid-Labile Subunit Deficiency	46	16.123

2	c	BLD140	Blood Group, I System	37	0.420

3		ACR007	Acromegaly	70	0.214

4		INS024	Insulin-Like Growth Factor I	83	0.209

5		PRS047	Prostatitis	59	0.158

6	P	PRS040	Prostate Cancer	88	0.151

7		END072	Endotheliitis	46	0.150

8	P	HPT021	Hepatitis	75	0.141

9		AGN016	Aging	65	0.138

10	P	DBT009	Diabetes Mellitus	72	0.136

11		GRW007	Growth Hormone Deficiency	52	0.126

12	P	CLR023	Colorectal Cancer	98	0.123

13		BDY004	Body Mass Index Quantitative Trait Locus 11	75	0.119

14		BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.119

15		BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.119

16		BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.119

17		BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.119

18		BDY010	Body Mass Index Quantitative Trait Locus 4	45	0.119

19		BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.119

20		BDY006	Body Mass Index Quantitative Trait Locus 8	42	0.119

21		BDY012	Body Mass Index Quantitative Trait Locus 7	42	0.119

22	P	HYP086	Hypothyroidism	62	0.117

23		SND001	Sandhoff Disease	65	0.106

24		LRN002	Laron Syndrome	63	0.103

25	P	HYP083	Hypopituitarism	59	0.103

26		MMM006	Mammographic Density	43	0.103

27	c	MLT151	Multiple Mitochondrial Dysfunctions Syndrome 5	36	0.102

28	c	HPT001	Hepatitis C	73	0.100

29	c	HPT073	Hepatitis C Virus	73	0.098

30	P	HRT032	Heart Disease	80	0.086

31	P	LPS004	Lupus Erythematosus	69	0.086

32	P	ANR048	Aniridia 1	68	0.086

33	c	SYS001	Systemic Lupus Erythematosus	86	0.083

34		SHW002	Shwachman-Diamond Syndrome	63	0.083

35		PNL019	Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities	53	0.083

36		ANR038	Anorexia Nervosa 1	21	0.083

37	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	21	0.083

38		BLD137	Blood Group--Ahonen	17	0.083

39		MLT157	Multiple System Atrophy 1	65	0.078

40		HYP056	Hypoglycemia	62	0.078

41	P	STS008	Sotos Syndrome 1	56	0.078

42	c	CNT075	Central Precocious Puberty	52	0.078

43	P	PRC019	Precocious Puberty	52	0.078

44	P	TRN020	Turner Syndrome	69	0.073

45	P	CRN300	Coronary Heart Disease 1	57	0.073

46	P	SLV001	Silver-Russell Syndrome	57	0.073

47		BRN106	Burns	57	0.073

48		ISL001	Islet Cell Tumor	54	0.073

49	c	OST164	Osteoporosis, Juvenile	54	0.073

50	c	BLM008	Bulimia Nervosa 2	53	0.073

51		OST016	Osteochondrosis	52	0.073

52		CMP034	Complete Androgen Insensitivity Syndrome	47	0.073

53	c	PTT056	Pituitary Adenoma 1, Multiple Types	46	0.073

54		FTL021	Fetal Macrosomia	46	0.073

55		ISL015	Isolated Growth Hormone Deficiency, Type Ib	44	0.073

56		HYP070	Hyperpituitarism	43	0.073

57	P	SLL003	Salla Disease	43	0.073

58		DFF006	Diffuse Idiopathic Skeletal Hyperostosis	42	0.073

59	c	SCN052	Secondary Adrenal Insufficiency	41	0.073

60		MNN006	Meninges Hemangiopericytoma	39	0.073

61		PSD008	Pseudopapilledema	37	0.073

62		SLP010	Slipped Capital Femoral Epiphysis	37	0.073

63		FST010	Fasting Hypoglycemia	36	0.073

64		OCL004	Ocular Hyperemia	31	0.073

65		ALR002	Al-Raqad Syndrome	30	0.073

66		GRW003	Growth Hormone Insensitivity with Immunodeficiency	21	0.073