Search results for Porphobilinogen

58 hits were found for Porphobilinogen

#	Family	MCID	Name	MIFTS	Score
1		PRP083	Porphyria, Acute Intermittent	64	6.866

2	P	PRP056	Porphyria, Acute Hepatic	48	6.386

3	P	PRP029	Porphyria	62	0.885

4	c	ACT078	Acute Porphyria	51	0.376

5		VRG001	Variegate Porphyria	56	0.183

6	P	PRP003	Porphyria Cutanea Tarda	67	0.171

7	P	LKM002	Leukemia	68	0.129

8		ERY051	Erythroleukemia, Familial	56	0.129

9	P	SCH015	Schizophrenia	74	0.112

10		IRN002	Iron Metabolism Disease	57	0.112

11		CTN011	Cutaneous Porphyria	38	0.112

12		DFC004	Deficiency Anemia	70	0.091

13	P	LVR013	Liver Disease	68	0.091

14	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.091

15	P	GLM045	Glioma	63	0.091

16		LVR012	Liver Cirrhosis	62	0.091

17	P	ENC018	Encephalopathy	61	0.091

18		CPR004	Coproporphyria, Hereditary	57	0.091

19	P	NRP001	Neuropathy	56	0.091

20		PRP082	Porphyria, Congenital Erythropoietic	56	0.091

21		47X002	47,xyy	49	0.091

22		GLL048	Glial Tumor	45	0.091

23		48X005	48,xyyy	39	0.091

24	P	HPT023	Hepatocellular Carcinoma	100	0.065

25	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.065

26		SCK003	Sickle Cell Anemia	74	0.065

27	P	MLT020	Multiple Sclerosis	72	0.065

28		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.065

29		PLM031	Poliomyelitis	64	0.065

30	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.065

31	P	THL005	Thalassemia	60	0.065

32		DBN001	Dubin-Johnson Syndrome	59	0.065

33	P	BRS044	Breast Adenocarcinoma	59	0.065

34		IRN001	Iron Deficiency Anemia	59	0.065

35	P	GLL022	Guillain-Barre Syndrome	59	0.065

36	c	ACT073	Acute Leukemia	58	0.065

37	P	TYR004	Tyrosinemia	58	0.065

38		CNS004	Constipation	58	0.065

39	P	PRP019	Peripheral Nervous System Disease	58	0.065

40	P	PLY019	Polyneuropathy	56	0.065

41		PRN011	Pernicious Anemia	53	0.065

42		SCH012	Schizoaffective Disorder	50	0.065

43		URM002	Uremia	49	0.065

44		SPL018	Splenomegaly	48	0.065

45	P	MRC003	Mercury Poisoning	48	0.065

46		HLX001	Helix Syndrome	47	0.065

47	c	INH020	Inherited Metabolic Disorder	47	0.065

48		LYM019	Lymphosarcoma	46	0.065

49	P	BNG032	Benign Mesothelioma	46	0.065

50	P	SPR119	Spermatogenic Failure, X-Linked, 1	39	0.065

51	P	DYS021	Dysautonomia	39	0.065

52	P	AXN001	Axonal Neuropathy	36	0.065

53		CHR178	Chromosomal Triplication	35	0.065

54		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.065

55	c	FML324	Familial Porphyria Cutanea Tarda	31	0.065

56		ARG004	Argyria	27	0.065

57		CHS007	Chester Porphyria	15	0.065

58		ANM041	Anemia, Nonspherocytic Hemolytic, Possibly Due to Defect in Porphyrin Metabolism	8	0.065