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
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