Search results for FAH

48 hits were found for FAH

# Family MCID Name MIFTS Score
1
c TYR012 Tyrosinemia, Type I 66 23.171
2
P TYR004 Tyrosinemia 58 5.573
3
P LVR013 Liver Disease 68 4.661
4
P HPT023 Hepatocellular Carcinoma 100 4.601
5
RCK004 Rickets 68 3.638
6
LVR012 Liver Cirrhosis 62 3.564
7
ALK013 Alkaptonuria 58 2.910
8
c TYR013 Tyrosinemia, Type Ii 47 2.910
9
P FNC004 Fanconi Syndrome 50 2.118
10
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 2.058
11
P CRG003 Crigler-Najjar Syndrome, Type I 63 2.058
12
URC002 Urea Cycle Disorder 51 2.058
13
c INF145 Infantile Liver Failure Syndrome 1 50 2.058
14
HWK001 Hawkinsinuria 42 2.058
15
HYP003 Hypermethioninemia 40 2.058
16
c TYR011 Tyrosinemia, Type Iii 40 2.058
17
AMN002 Amino Acid Metabolic Disorder 39 2.058
18
SVR004 Severe Combined Immunodeficiency 73 0.147
19
ATS010 Autosomal Recessive Disease 48 0.147
20
CNG034 Congestive Heart Failure 69 0.104
21
DSR026 Disorder of Tyrosine Metabolism 14 0.104
22
c HPT073 Hepatitis C Virus 72 0.073
23
P NRB001 Neuroblastoma 72 0.073
24
P TTR001 Tetralogy of Fallot 70 0.073
25
P MLN008 Melanoma 69 0.073
26
HYP056 Hypoglycemia 66 0.073
27
PRT036 Peritonitis 64 0.073
28
c HPT001 Hepatitis C 62 0.073
29
HPT019 Hepatic Encephalopathy 60 0.073
30
c HPT016 Hepatitis B 59 0.073
31
ANT024 Anthrax Disease 58 0.073
32
P INT070 Intestinal Obstruction 58 0.073
33
P EHL001 Ehlers-Danlos Syndrome 58 0.073
34
c ACT134 Acute Liver Failure 56 0.073
35
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.073
36
KRT009 Keratosis 51 0.073
37
ILS001 Ileus 51 0.073
38
HYP017 Hypophosphatemia 50 0.073
39
VLV047 Volvulus of Midgut 49 0.073
40
HPT004 Hepatic Coma 45 0.073
41
P HYP265 Hypotonia 43 0.073
42
P FNC034 Fanconi Renotubular Syndrome 2 40 0.073
43
P CRB088 Cerebral Atrophy 37 0.073
44
HYP007 Hypermobility Syndrome 36 0.073
45
CRB159 Cerebral Visual Impairment 35 0.073
47
HML018 Homologous Wasting Disease 22 0.073
48
FCL040 Focal Acral Hyperkeratosis 15 0.073
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