Search results for ass1

50 hits were found for ass1

#	Family	MCID	Name	MIFTS	Score
1		CTR172	Citrullinemia, Classic	64	7.494

2		ARG002	Argininosuccinic Aciduria	61	3.695

3	P	HPT023	Hepatocellular Carcinoma	100	3.603

4		LYS003	Lysinuric Protein Intolerance	57	3.120

5		ATS010	Autosomal Recessive Disease	48	2.696

6	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	57	2.631

7		HPT067	Hepatocellular Adenoma	44	2.631

8		ORT008	Orotic Aciduria	55	2.593

9		PHN003	Phenylketonuria	75	2.547

10	c	LKM063	Leukemia, Chronic Myeloid	72	2.547

11		PRP001	Propionic Acidemia	65	2.547

12		HPT019	Hepatic Encephalopathy	60	2.547

13		NLP001	Nail-Patella Syndrome	60	2.547

14		ORN008	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to	59	2.547

15		ARG007	Argininemia	57	2.547

16		CRB186	Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to	52	2.547

17		RYS001	Reye Syndrome	51	2.547

18		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	1.978

19		URC002	Urea Cycle Disorder	51	1.945

20	c	ADL083	Adult-Onset Citrullinemia Type I	10	1.861

21	c	ACT189	Acute Neonatal Citrullinemia Type I	8	1.861

22	P	LYN001	Lynch Syndrome	77	1.801

23	P	WRD001	Waardenburg's Syndrome	59	1.801

24		HYP774	Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome	55	1.801

25		AMN002	Amino Acid Metabolic Disorder	39	1.801

26		ACY011	Acyl-Coa Dehydrogenase Deficiency	38	1.801

27		BRN135	Branched-Chain Keto Acid Dehydrogenase Kinase Deficiency	38	1.801

28		PST103	Postpartum Psychosis	32	1.801

29		PYR035	Pyrimidine Metabolic Disorder	26	1.801

30		ADN018	Adenoma	59	0.143

31	P	ENC018	Encephalopathy	61	0.101

32		OCL069	Ocular Motor Apraxia	51	0.101

33		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.101

34		GLB015	Glioblastoma Multiforme	75	0.072

35	P	NSP012	Nasopharyngeal Carcinoma	66	0.072

36		CHL068	Cholestasis	61	0.072

37	P	THL005	Thalassemia	60	0.072

38	P	EPS003	Episodic Ataxia	59	0.072

39		CHR177	Chromophobe Renal Cell Carcinoma	57	0.072

40		HMG005	Hemoglobinopathy	56	0.072

41	P	ALP008	Alopecia	54	0.072

42	P	RNL017	Renal Oncocytoma	53	0.072

43		KRT009	Keratosis	51	0.072

44	P	SCK005	Sickle Cell Disease	50	0.072

45		HLX001	Helix Syndrome	47	0.072

46	c	INH020	Inherited Metabolic Disorder	47	0.072

47	P	BNG032	Benign Mesothelioma	46	0.072

48		MYX013	Myxofibrosarcoma	45	0.072

49	c	MLG079	Malignant Pleural Mesothelioma	42	0.072

50		PLY150	Polykaryocytosis Inducer	31	0.072