Search results for "myasthenia gravis, neonatal transient"

The MalaCard for "myasthenia gravis, neonatal transient" has been retired.
Searching MalaCards for entries containing "myasthenia gravis, neonatal transient"

172 hits were found for 'myasthenia gravis, neonatal transient'

# Family MCID Name MIFTS Score
1
c TRN062 Transient Neonatal Myasthenia Gravis 14 6.146
2
P MYS003 Myasthenia Gravis 64 1.266
3
CRB009 Cerebritis 36 0.359
4
P NNT006 Neonatal Myasthenia Gravis 24 0.307
5
P HYP086 Hypothyroidism 63 0.269
6
P MYP004 Myopathy 67 0.250
7
NRN002 Neuronitis 40 0.247
8
P HPT021 Hepatitis 74 0.237
9
P THY032 Thyroiditis 57 0.235
10
P LPS004 Lupus Erythematosus 63 0.231
11
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.208
12
P MNN013 Meningitis 66 0.201
13
PMP001 Pemphigus 49 0.200
14
c SYS001 Systemic Lupus Erythematosus 87 0.190
15
P LKM002 Leukemia 70 0.183
16
P ENC004 Encephalitis 60 0.165
17
P CRD011 Cardiomyopathy 66 0.164
18
P RSP003 Respiratory Failure 68 0.163
19
P NRV007 Nervous System Disease 71 0.155
20
P THR014 Thrombocytopenia 63 0.154
21
P CRV039 Cervicitis 45 0.150
22
P LYM118 Lymphoma 68 0.146
23
P ART022 Arthritis 73 0.145
24
PMP004 Pemphigus Foliaceus 42 0.144
25
P MYC008 Myocarditis 56 0.143
26
P HYP076 Hyperthyroidism 59 0.141
27
ANR040 Aneurysm 56 0.136
28
PRP030 Purpura 60 0.136
29
P GRV001 Graves' Disease 62 0.135
30
PRR002 Pure Red-Cell Aplasia 47 0.134
31
P PNC044 Pancreatitis 62 0.134
32
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.134
33
P ESP024 Esophagitis 62 0.130
34
P PNM007 Pneumonia 67 0.130
35
PYL006 Pyloric Stenosis 46 0.126
36
P PLY019 Polyneuropathy 53 0.126
37
P AST005 Asthma 80 0.123
38
P MSC005 Muscular Dystrophy 64 0.123
39
P CND004 Candidiasis 58 0.123
40
P MYC007 Myocardial Infarction 80 0.123
41
P NRP001 Neuropathy 57 0.121
42
C3D001 C3 Deficiency 50 0.120
43
ALR002 Al-Raqad Syndrome 36 0.120
44
MDS022 Mediastinitis 37 0.119
45
SRC014 Sarcoma 66 0.118
46
ALP008 Alopecia 56 0.118
47
c HPT001 Hepatitis C 68 0.118
48
ADN018 Adenoma 59 0.118
49
P ANT006 Antiphospholipid Syndrome 60 0.117
50
DRM006 Dermatitis 58 0.116
51
CYT008 Cytomegalovirus Infection 51 0.115
52
TTN003 Tetanus 62 0.111
53
P HML002 Hemolytic Anemia 60 0.110
54
P CHL066 Cholangitis 48 0.109
55
MTB004 Metabolic Acidosis 49 0.109
56
P DMY001 Demyelinating Polyneuropathy 41 0.108
57
P RHM011 Rheumatoid Arthritis 87 0.107
58
MYT011 Myotonia 40 0.107
59
PRS047 Prostatitis 56 0.107
60
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.105
61
GTR002 Goiter 54 0.105
62
P DRR001 Diarrhea 60 0.104
63
P TXP001 Toxoplasmosis 61 0.103
64
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 38 0.103
65
MLN008 Melanoma 61 0.103
66
P GLM007 Glomerulonephritis 56 0.100
67
P MYT002 Myotonic Dystrophy 46 0.100
68
P CNJ013 Conjunctivitis 65 0.100
69
DYS073 Dysphagia 51 0.100
70
THR004 Thrombocytosis 55 0.100
71
P HMP007 Hemophilia 55 0.099
72
P PLM037 Pulmonary Hypertension 78 0.099
73
SVR004 Severe Combined Immunodeficiency 71 0.097
74
c ATM003 Autoimmune Thyroiditis 59 0.097
75
LMB024 Limbic Encephalitis 35 0.096
76
P HYP024 Hypoparathyroidism 52 0.096
77
P TRN034 Transverse Myelitis 43 0.095
78
P PMP005 Pemphigus Vulgaris 47 0.095
79
P DYS021 Dysautonomia 47 0.094
80
P PRT013 Portal Hypertension 61 0.093
81
TBR010 Tuberculosis 70 0.092
82
PRN011 Pernicious Anemia 41 0.092
83
P OBS005 Obesity 91 0.091
84
P CTR002 Cataract 57 0.091
85
P SCL009 Sclerosing Cholangitis 47 0.091
86
MYL001 Myelitis 35 0.090
87
CCN007 Cocoon Syndrome 32 0.090
88
P APL001 Aplastic Anemia 74 0.090
89
ART016 Aortic Aneurysm 67 0.090
90
CNN005 Connective Tissue Disease 60 0.089
91
P SCH015 Schizophrenia 78 0.089
92
P LYM026 Lymphoblastic Leukemia 60 0.089
93
P DYS154 Dystonia 62 0.089
94
TTH006 Tooth Disease 52 0.088
95
P UVT001 Uveitis 60 0.087
96
MYX004 Myxedema 36 0.087
97
AYM001 Ayme-Gripp Syndrome 40 0.087
98
PLY012 Polyhydramnios 45 0.086
99
P SLP006 Sleep Apnea 60 0.086
100
CRD137 Cardiogenic Shock 44 0.086
101
P BRS047 Breast Cancer 100 0.086
102
ADR008 Adrenal Adenoma 49 0.086
103
PRC012 Pericardial Effusion 50 0.086
104
c HMP029 Hemophilia a 61 0.085
105
URT039 Urticaria 58 0.085
106
RHB003 Rhabdomyosarcoma 55 0.085
107
P CRN035 Cranial Nerve Palsy 44 0.085
108
FSC004 Fasciitis 47 0.085
109
CCN002 Cocaine Abuse 47 0.085
110
DPH001 Diphtheria 55 0.084
111
P NPH012 Nephrotic Syndrome 55 0.084
112
P CTN003 Cutaneous Lupus Erythematosus 49 0.084
113
P CLR023 Colorectal Cancer 96 0.084
114
ASP003 Aseptic Meningitis 51 0.083
115
P GST044 Gastritis 64 0.082
116
OTP003 Oto-Palatal-Digital Syndrome 14 0.082
117
P PLM036 Pulmonary Fibrosis 69 0.082
118
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.081
119
HMT018 Hematopoietic Stem Cell Transplantation 39 0.081
120
BLD054 Blood Protein Disease 38 0.081
121
STS002 Situs Inversus 43 0.080
122
P CLC005 Celiac Disease 67 0.079
123
c ATM010 Autoimmune Hemolytic Anemia 59 0.079
124
P LCH002 Lichen Planus 61 0.079
125
P PRM006 Primary Biliary Cirrhosis 55 0.079
126
HPT074 Hepatic Adenoma, Somatic 35 0.078
127
CRC006 Carcinoid Syndrome 51 0.077
128
BRN002 Bronchiolitis 56 0.077
129
MXD005 Mixed Connective Tissue Disease 63 0.076
130
WTH001 Withdrawal Disorder 36 0.075
131
P AMY004 Amyloidosis 63 0.074
132
CHR001 Churg-Strauss Syndrome 48 0.074
133
NRT004 Neuritis 52 0.074
134
CRT009 Critical Illness Polyneuropathy 38 0.074
135
P NRV006 Nervous System Cancer 62 0.074
136
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.073
137
PRT029 Parathyroid Adenoma 46 0.072
138
ATM074 Autoimmune Autonomic Ganglionopathy 18 0.072
139
VND001 Vein Disease 51 0.072
140
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.072
141
P HYP098 Hypereosinophilic Syndrome 48 0.072
142
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 37 0.072
143
GRN017 Granulocytopenia 39 0.072
144
CHR063 Chronic Mucocutaneous Candidiasis 61 0.071
145
BRN012 Bronchiolitis Obliterans 58 0.071
146
ORL013 Oral Lichen Planus 53 0.071
147
ATN004 Autonomic Neuropathy 44 0.071
148
LPD004 Lipoid Nephrosis 49 0.071
149
EST005 Esotropia 39 0.068
150
NRF007 Neurofibroma 53 0.068
151
MMB002 Membranous Glomerulonephritis 47 0.068
152
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.068
153
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.068
154
PST055 Postural Hypotension 36 0.068
155
SKN023 Skin Tag 48 0.067
156
OPT006 Optic Nerve Disease 47 0.066
157
FST001 Foster-Kennedy Syndrome 31 0.066
158
LKC003 Leukocyte Disease 45 0.066
159
P INF032 Infertility 61 0.065
160
ASB001 Asbestosis 42 0.064
161
MLT001 Multiple Chemical Sensitivity 43 0.064
162
SWL001 Swallowing Disorders 33 0.062
163
c PLM128 Pulmonary Hypertension, Primary, 2 36 0.060
164
c PRM023 Pre-Malignant Neoplasm 42 0.058
165
DSS008 Disease of Mental Health 48 0.058
166
THY030 Thyroid Gland Disease 52 0.054
167
CNT098 Central Core Disease 68 0.048
168
CRH001 Crohn's Disease 76 0.048
169
INC022 Inclusion-Cell Disease 46 0.046
170
LYM024 Lymphatic System Disease 49 0.046
171
c PLM127 Pulmonary Hypertension, Primary, 3 31 0.046
172
RPR002 Reproductive System Disease 45 0.046