Search results for Carbamoyl phosphate

164 hits were found for Carbamoyl phosphate

# Family MCID Name MIFTS Score
1
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 52 14.836
2
NTR005 Nutritional Deficiency Disease 62 3.384
3
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.283
4
P KDN018 Kidney Disease 72 0.230
5
c CHR684 Chronic Kidney Disease 70 0.227
6
HYP017 Hypophosphatemia 50 0.220
7
END086 End Stage Renal Disease 51 0.207
8
URM002 Uremia 49 0.175
9
P MYL006 Myeloid Leukemia 60 0.157
10
OCL069 Ocular Motor Apraxia 51 0.153
11
c LKM061 Leukemia, Acute Myeloid 84 0.151
12
URC002 Urea Cycle Disorder 51 0.144
13
LVR012 Liver Cirrhosis 62 0.135
14
P LVR013 Liver Disease 68 0.133
15
OST159 Osteogenic Sarcoma 66 0.131
16
P ENC018 Encephalopathy 61 0.128
17
ATS010 Autosomal Recessive Disease 48 0.119
18
P GLM045 Glioma 63 0.118
19
GLL048 Glial Tumor 45 0.118
20
P NRB001 Neuroblastoma 72 0.116
21
P PRS040 Prostate Cancer 97 0.115
22
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.110
23
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.107
24
HRW001 Hair Whorl 36 0.105
25
P NRP001 Neuropathy 56 0.101
26
P ADN016 Adenocarcinoma 64 0.100
27
47X002 47,xyy 49 0.099
28
HMN044 Human Immunodeficiency Virus Type 1 71 0.096
29
CHL014 Cholera 59 0.095
30
GLB015 Glioblastoma Multiforme 75 0.094
31
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.093
32
P RSP003 Respiratory Failure 74 0.090
33
NCT003 N-Acetylglutamate Synthase Deficiency 45 0.090
34
MLR004 Malaria 81 0.090
35
P DRR001 Diarrhea 55 0.089
36
ENT011 Enterocolitis 51 0.089
37
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.088
38
HMP009 Haemophilus Influenzae 43 0.088
39
PRN019 Perinatal Necrotizing Enterocolitis 59 0.087
40
HYP056 Hypoglycemia 66 0.086
41
VSL002 Visual Epilepsy 59 0.085
42
P SZR006 Seizure Disorder 56 0.085
43
ADN018 Adenoma 59 0.084
44
c INH020 Inherited Metabolic Disorder 47 0.083
45
IMM167 Immune Deficiency Disease 78 0.082
46
P FBR017 Fibrosarcoma 56 0.080
47
P ANP001 Anaplastic Large Cell Lymphoma 58 0.080
48
ORT008 Orotic Aciduria 55 0.076
49
SVR004 Severe Combined Immunodeficiency 73 0.075
50
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.074
51
P HPT023 Hepatocellular Carcinoma 100 0.074
52
STR067 Stroke, Ischemic 81 0.074
53
CRB039 Cerebrovascular Disease 67 0.074
54
P HRP006 Herpes Simplex 65 0.073
55
THY029 Thyroid Carcinoma 59 0.073
56
FTT001 Fatty Liver Disease 61 0.071
57
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.070
58
DPR016 Depression 63 0.070
59
SPN186 Spinal Cord Injury 60 0.069
60
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.069
61
P HYP265 Hypotonia 43 0.069
62
P SCK005 Sickle Cell Disease 50 0.068
63
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.066
64
P BLD134 Bladder Cancer 79 0.066
65
c HYP836 Hypercholesterolemia, Familial, 1 73 0.066
66
PRT036 Peritonitis 64 0.066
67
ATM095 Autoimmune Disease 62 0.066
68
MNT002 Mental Depression 58 0.066
69
END057 Endometrial Cancer 74 0.065
70
P CRB088 Cerebral Atrophy 37 0.065
71
PLM124 Pulmonary Hypertension, Neonatal 19 0.063
72
P MLT020 Multiple Sclerosis 72 0.063
73
P TXP001 Toxoplasmosis 60 0.063
74
BRN004 Brain Edema 56 0.063
75
c VRL010 Viral Hepatitis 52 0.063
76
ALL014 Allergic Encephalomyelitis 38 0.063
77
c MGR028 Migraine with or Without Aura 1 67 0.061
78
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.061
79
P SPP010 Suppressor of Tumorigenicity 3 51 0.061
80
HPT004 Hepatic Coma 45 0.061
81
c PCH010 Pachyonychia Congenita 3 44 0.061
82
P PLM037 Pulmonary Hypertension 67 0.060
83
c HPT001 Hepatitis C 62 0.060
84
HPT019 Hepatic Encephalopathy 60 0.060
85
HYP060 Hyperinsulinism 54 0.060
86
GLC003 Glucose Intolerance 54 0.060
87
PRP001 Propionic Acidemia 65 0.060
88
P DBT005 Diabetes Insipidus 55 0.060
89
ORG002 Organic Acidemia 44 0.060
90
c 3MT007 3-Methylglutaconic Aciduria 36 0.060
91
CLF027 Cleft Palate, Isolated 64 0.058
92
ANR007 Anorexia Nervosa 63 0.058
93
P TRC086 Trichohepatoenteric Syndrome 1 62 0.058
94
P BRS044 Breast Adenocarcinoma 59 0.058
95
c ACT134 Acute Liver Failure 56 0.058
96
P HMC002 Homocystinuria 53 0.058
97
RYS001 Reye Syndrome 51 0.058
98
c SPN225 Spondyloarthropathy 1 73 0.057
99
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.057
100
THR013 Thoracic Outlet Syndrome 54 0.057
101
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.057
102
P ALZ034 Alzheimer Disease 88 0.055
103
P ANG001 Angelman Syndrome 69 0.055
104
P MJR001 Major Depressive Disorder 68 0.055
105
PSY004 Psychotic Disorder 67 0.055
106
BRR014 Barrett Esophagus 65 0.055
107
SCH014 Schistosomiasis 57 0.055
108
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.055
109
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.055
110
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.053
111
IRR002 Irritable Bowel Syndrome 65 0.053
112
P ANR048 Aniridia 1 63 0.053
113
ACN002 Acanthosis Nigricans 60 0.053
114
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.053
115
RNL077 Renal Fibrosis 47 0.053
116
PRM020 Premenstrual Tension 40 0.053
117
ATX010 Ataxia Neuropathy Spectrum 34 0.053
118
ACT064 Acute Necrotizing Encephalitis 33 0.053
119
BLD137 Blood Group--Ahonen 16 0.053
120
CHL065 Cholangiocarcinoma 68 0.051
121
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.051
122
AND002 Androgen Insensitivity Syndrome 66 0.051
123
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.051
124
MYC088 Mycobacterium Avium Complex Infections 29 0.051
125
c PNC108 Pancreatitis, Hereditary 70 0.049
126
P AXN002 Axenfeld-Rieger Syndrome 59 0.049
127
GNR004 Generalized Anxiety Disorder 56 0.049
128
GLS001 Gliosarcoma 54 0.049
129
P INT068 Intestinal Disease 53 0.049
130
INT079 Intrahepatic Cholangiocarcinoma 51 0.049
131
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.049
132
ALR002 Al-Raqad Syndrome 33 0.049
133
P VSC018 Visceral Steatosis 33 0.049
134
CYN003 Cyanide Poisoning 24 0.049
135
AND005 Androgen Insensitivity Syndrome, Mild 19 0.049
136
c TYR012 Tyrosinemia, Type I 66 0.046
137
LSC001 Lesch-Nyhan Syndrome 62 0.046
138
ARG002 Argininosuccinic Aciduria 61 0.046
139
P LKD001 Leukodystrophy 59 0.046
140
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.046
141
ARG007 Argininemia 57 0.046
142
c SML009 Small Intestine Adenocarcinoma 57 0.046
143
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 0.046
144
LRN003 Learning Disability 49 0.046
145
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.046
146
MST004 Mast Cell Neoplasm 42 0.046
147
PLY100 Polyploidy 40 0.046
148
EXT007 Extracutaneous Mastocytoma 38 0.046
149
PST103 Postpartum Psychosis 32 0.046
150
WLS001 Wilson Disease 71 0.042
151
CTR172 Citrullinemia, Classic 64 0.042
152
LYS003 Lysinuric Protein Intolerance 57 0.042
153
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.042
154
ISV001 Isovaleric Acidemia 55 0.042
155
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.042
156
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.042
157
DDN006 Duodenitis 49 0.042
158
STR103 Streptococcus Pneumonia 47 0.042
159
AMN002 Amino Acid Metabolic Disorder 39 0.042
160
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.042
161
CRB009 Cerebritis 37 0.042
162
CHR387 Chromosome Xp21 Deletion Syndrome 35 0.042
163
MYC019 Mycobacterium Marinum 29 0.042
164
PYR035 Pyrimidine Metabolic Disorder 26 0.042
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