Search results for nags

148 hits were found for nags

# Family MCID Name MIFTS Score
1
NCT003 N-Acetylglutamate Synthase Deficiency 45 22.387
2
ASP002 Aspartylglucosaminuria 62 6.855
3
URC002 Urea Cycle Disorder 51 2.701
4
PRP001 Propionic Acidemia 65 2.615
5
c INH020 Inherited Metabolic Disorder 47 2.615
6
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.042
7
P MPL001 Maple Syrup Urine Disease 69 1.849
8
c TYR012 Tyrosinemia, Type I 66 1.849
9
P CLC063 Celiac Disease 1 66 1.849
10
CTR172 Citrullinemia, Classic 64 1.849
11
ARG002 Argininosuccinic Aciduria 61 1.849
12
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 1.849
13
ARG007 Argininemia 57 1.849
14
LYS003 Lysinuric Protein Intolerance 57 1.849
15
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 1.849
16
ISV001 Isovaleric Acidemia 55 1.849
17
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 1.849
18
ORT008 Orotic Aciduria 55 1.849
19
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 1.849
20
CRB186 Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to 52 1.849
21
P MTH008 Methylmalonic Acidemia 50 1.849
22
c NLX003 Neu-Laxova Syndrome 2 47 1.849
23
ORG002 Organic Acidemia 44 1.849
24
AMN002 Amino Acid Metabolic Disorder 39 1.849
25
GRN006 Granulomatous Angiitis 30 1.849
26
PYR035 Pyrimidine Metabolic Disorder 26 1.849
27
CHL014 Cholera 59 0.274
28
P KDN018 Kidney Disease 72 0.175
29
c MCR113 Microvascular Complications of Diabetes 3 52 0.139
30
c MCR120 Microvascular Complications of Diabetes 7 47 0.139
31
c MCR130 Microvascular Complications of Diabetes 6 41 0.139
32
c MCR133 Microvascular Complications of Diabetes 4 41 0.139
33
P DBT009 Diabetes Mellitus 64 0.129
34
P NPH012 Nephrotic Syndrome 60 0.118
35
c ACT071 Acute Kidney Failure 60 0.118
36
c SYS001 Systemic Lupus Erythematosus 86 0.105
37
P NRB001 Neuroblastoma 72 0.105
38
c ACT068 Acute Cystitis 63 0.105
39
P GLM007 Glomerulonephritis 57 0.105
40
P LVR013 Liver Disease 68 0.091
41
HYD002 Hydronephrosis 60 0.091
42
P PNC025 Panic Disorder 53 0.091
43
47X002 47,xyy 49 0.091
44
HLX001 Helix Syndrome 47 0.091
45
DFC004 Deficiency Anemia 70 0.075
46
c PRC016 Pre-Eclampsia 63 0.075
47
ESP020 Esophageal Atresia 62 0.075
48
P LPS004 Lupus Erythematosus 61 0.075
49
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.075
50
SPN186 Spinal Cord Injury 60 0.075
51
ISC004 Ischemia 58 0.075
52
c VSC019 Vesicoureteral Reflux 1 57 0.075
53
P PYL005 Pyelonephritis 56 0.075
54
P MLN007 Male Infertility 55 0.075
55
P DRR001 Diarrhea 55 0.075
56
NPH009 Nephrolithiasis 55 0.075
57
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.075
58
P INT068 Intestinal Disease 53 0.075
59
NPH003 Nephrocalcinosis 51 0.075
60
OCL069 Ocular Motor Apraxia 51 0.075
61
END086 End Stage Renal Disease 51 0.075
62
PYL006 Pyloric Stenosis 48 0.075
63
URL001 Urolithiasis 45 0.075
64
c HYP595 Hypertension, Essential 84 0.053
65
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.053
66
P RHM011 Rheumatoid Arthritis 80 0.053
67
c NRF023 Neurofibromatosis, Type Ii 80 0.053
68
OST012 Osteoarthritis 78 0.053
69
SCK003 Sickle Cell Anemia 74 0.053
70
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.053
71
P TYS001 Tay-Sachs Disease 69 0.053
72
P PNM007 Pneumonia 68 0.053
73
SKN019 Skin Melanoma 68 0.053
74
P HYP098 Hypereosinophilic Syndrome 67 0.053
75
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.053
76
HYP056 Hypoglycemia 66 0.053
77
c DBT099 Diabetes Mellitus, Type I 65 0.053
78
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.053
79
GT001 Gout 64 0.053
80
c FNC043 Fanconi Anemia, Complementation Group E 62 0.053
81
P ESP024 Esophagitis 62 0.053
82
ALL026 Allergic Hypersensitivity Disease 62 0.053
83
CRN239 Carnitine Deficiency, Systemic Primary 62 0.053
84
MDD011 Mood Disorder 62 0.053
85
TXC005 Toxic Shock Syndrome 62 0.053
86
FTT001 Fatty Liver Disease 61 0.053
87
P ENC018 Encephalopathy 61 0.053
88
PRN019 Perinatal Necrotizing Enterocolitis 59 0.053
89
P MLN069 Melanoma, Uveal 59 0.053
90
P CYS018 Cystitis 59 0.053
91
IRN001 Iron Deficiency Anemia 59 0.053
92
GST045 Gastroenteritis 59 0.053
93
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.053
94
P BCL017 B-Cell Lymphoma 58 0.053
95
P INF032 Infertility 57 0.053
96
IRN002 Iron Metabolism Disease 57 0.053
97
CHK001 Chikungunya 57 0.053
98
P HDC001 Headache 57 0.053
99
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.053
100
c ACT075 Acute Myocardial Infarction 57 0.053
101
P END033 Endocarditis 57 0.053
102
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.053
103
PLC005 Placental Insufficiency 57 0.053
104
SCH014 Schistosomiasis 57 0.053
105
HMT008 Hematuria, Benign Familial 56 0.053
106
BCT022 Bacterial Infectious Disease 56 0.053
107
PRS047 Prostatitis 56 0.053
108
P GRV001 Graves' Disease 55 0.053
109
URN010 Urinary Tract Obstruction 55 0.053
110
NRT001 Neurotic Disorder 53 0.053
111
DYS015 Dysentery 52 0.053
112
P THY032 Thyroiditis 52 0.053
113
HYP014 Hyperuricemia 52 0.053
114
PPT001 Peptic Esophagitis 52 0.053
115
ENT011 Enterocolitis 51 0.053
116
HYP781 Hypoascorbemia 51 0.053
117
P OVR082 Overgrowth Syndrome 50 0.053
118
OCL022 Ocular Melanoma 50 0.053
119
INT017 Intestinal Schistosomiasis 48 0.053
120
ATS010 Autosomal Recessive Disease 48 0.053
121
P RNV001 Renovascular Hypertension 48 0.053
122
URN003 Urinary Schistosomiasis 46 0.053
123
c ACT042 Acute Pyelonephritis 46 0.053
124
P HYP733 Hypercalciuria, Absorptive, 2 45 0.053
125
c SBC007 Subacute Thyroiditis 45 0.053
126
AGR002 Agoraphobia 45 0.053
127
DBT008 Diabetic Angiopathy 44 0.053
128
CLN003 Clonorchiasis 44 0.053
129
BCT021 Bacterial Sepsis 44 0.053
130
URT037 Urethral Stricture 43 0.053
131
IDP073 Idiopathic Hypercalciuria 43 0.053
132
IDP091 Idiopathic Nephrotic Syndrome 42 0.053
133
LTX001 Latex Allergy 41 0.053
134
NNT008 Neonatal Abstinence Syndrome 41 0.053
135
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.053
136
ANX004 Anoxia 40 0.053
137
PYR004 Pyuria 40 0.053
138
WLL004 Wallerian Degeneration 39 0.053
139
48X005 48,xyyy 39 0.053
140
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.053
141
ESN006 Eosinophilic Meningitis 38 0.053
142
ENT003 Enterobiasis 38 0.053
143
GLM044 Glomerular Disease 37 0.053
144
BLN010 Balanitis 37 0.053
145
BLN002 Balanitis Xerotica Obliterans 29 0.053
146
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.053
147
LKP001 Leukoplakia of Penis 25 0.053
148
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.053
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