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"

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

# Family MCID Name MIFTS Score
1
c TRN062 Transient Neonatal Myasthenia Gravis 15 6.141
2
P MYS003 Myasthenia Gravis 67 1.290
3
P THY023 Thymoma 57 0.425
4
CRB009 Cerebritis 39 0.351
5
P NNT006 Neonatal Myasthenia Gravis 24 0.306
6
P HYP086 Hypothyroidism 64 0.261
7
P MYP004 Myopathy 67 0.254
8
NRN002 Neuronitis 41 0.241
9
NRM005 Neuromuscular Disease 56 0.232
10
P HPT021 Hepatitis 69 0.229
11
P THY032 Thyroiditis 54 0.229
12
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.222
13
P LPS004 Lupus Erythematosus 64 0.215
14
PMP001 Pemphigus 50 0.197
15
P MNN013 Meningitis 67 0.193
16
P LKM002 Leukemia 71 0.178
17
c SYS001 Systemic Lupus Erythematosus 86 0.171
18
P RSP003 Respiratory Failure 71 0.159
19
P ENC004 Encephalitis 63 0.159
20
P CRD011 Cardiomyopathy 68 0.158
21
P THR014 Thrombocytopenia 64 0.143
22
P CRV039 Cervicitis 45 0.143
23
P LYM118 Lymphoma 69 0.142
24
PMP004 Pemphigus Foliaceus 42 0.138
25
P ART022 Arthritis 75 0.136
26
P MYC008 Myocarditis 54 0.135
27
P NRV007 Nervous System Disease 71 0.134
28
ANR040 Aneurysm 57 0.134
29
MSC004 Muscle Tissue Disease 34 0.133
30
P GRV001 Graves' Disease 59 0.132
31
P HYP076 Hyperthyroidism 55 0.132
32
P CNG001 Congenital Myasthenic Syndrome 55 0.128
33
PRR002 Pure Red-Cell Aplasia 47 0.126
34
PRP030 Purpura 58 0.125
35
P PNC044 Pancreatitis 61 0.124
36
P MSC005 Muscular Dystrophy 65 0.123
37
P PLY019 Polyneuropathy 56 0.122
38
MDS022 Mediastinitis 41 0.122
39
P ESP024 Esophagitis 61 0.121
40
P PNM007 Pneumonia 68 0.119
41
P NRP001 Neuropathy 59 0.114
42
P CND004 Candidiasis 57 0.114
43
P MYC007 Myocardial Infarction 79 0.113
44
SRC014 Sarcoma 66 0.112
45
P AST005 Asthma 82 0.112
46
c HPT001 Hepatitis C 68 0.112
47
ADN018 Adenoma 58 0.108
48
ALP008 Alopecia 57 0.107
49
CYT008 Cytomegalovirus Infection 52 0.106
50
WTH001 Withdrawal Disorder 37 0.106
51
P CHL066 Cholangitis 42 0.104
52
P ANT006 Antiphospholipid Syndrome 56 0.104
53
P DMY001 Demyelinating Polyneuropathy 43 0.103
54
DRM006 Dermatitis 66 0.103
55
PYL006 Pyloric Stenosis 46 0.102
56
GTR002 Goiter 52 0.101
57
P NRM001 Neuromyelitis Optica 60 0.101
58
MYT011 Myotonia 36 0.101
59
TTN003 Tetanus 61 0.100
60
INT042 Internuclear Ophthalmoplegia 37 0.100
61
P HML002 Hemolytic Anemia 62 0.099
62
PRS047 Prostatitis 56 0.099
63
P RHM011 Rheumatoid Arthritis 89 0.098
64
MTB004 Metabolic Acidosis 48 0.098
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.098
66
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.097
67
P GLM007 Glomerulonephritis 59 0.097
68
P PLM037 Pulmonary Hypertension 79 0.096
69
P TXP001 Toxoplasmosis 61 0.095
70
MLN008 Melanoma 62 0.094
71
TBR010 Tuberculosis 70 0.094
72
MYL001 Myelitis 51 0.093
73
P TRN034 Transverse Myelitis 49 0.093
74
P DRR001 Diarrhea 60 0.092
75
ALR002 Al-Raqad Syndrome 36 0.092
76
P MYT002 Myotonic Dystrophy 48 0.092
77
DYS073 Dysphagia 48 0.092
78
CCN007 Cocoon Syndrome 45 0.092
79
P CNJ013 Conjunctivitis 64 0.091
80
IMM136 Immune System Disease 51 0.091
81
ART016 Aortic Aneurysm 69 0.089
82
SVR004 Severe Combined Immunodeficiency 69 0.088
83
P PRT013 Portal Hypertension 60 0.088
84
P PMP005 Pemphigus Vulgaris 51 0.086
85
P HMP007 Hemophilia 57 0.086
86
P SCL009 Sclerosing Cholangitis 48 0.085
87
C3D001 C3 Deficiency 53 0.085
88
CNN005 Connective Tissue Disease 62 0.084
89
P DYS021 Dysautonomia 44 0.084
90
THR004 Thrombocytosis 55 0.084
91
P OBS005 Obesity 92 0.083
92
MYX004 Myxedema 35 0.082
93
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.082
94
OPT006 Optic Nerve Disease 52 0.082
95
FST001 Foster-Kennedy Syndrome 31 0.082
96
P ALP009 Alopecia Areata 62 0.081
97
ASP003 Aseptic Meningitis 51 0.080
98
P LYM026 Lymphoblastic Leukemia 62 0.080
99
P SCH015 Schizophrenia 77 0.079
100
BLD054 Blood Protein Disease 37 0.079
101
P UVT001 Uveitis 58 0.079
102
PLY020 Polyradiculoneuropathy 45 0.079
103
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.079
104
P CTR002 Cataract 58 0.078
105
P NPH012 Nephrotic Syndrome 59 0.078
106
TTH006 Tooth Disease 52 0.078
107
FSC004 Fasciitis 48 0.078
108
P CRN035 Cranial Nerve Palsy 46 0.078
109
URT039 Urticaria 57 0.077
110
RHB003 Rhabdomyosarcoma 57 0.077
111
MCS002 Mucositis 55 0.076
112
CRD137 Cardiogenic Shock 46 0.075
113
PLY012 Polyhydramnios 47 0.075
114
P CTN003 Cutaneous Lupus Erythematosus 48 0.075
115
DPH001 Diphtheria 59 0.075
116
P SLP006 Sleep Apnea 61 0.074
117
LPD004 Lipoid Nephrosis 48 0.074
118
P DYS154 Dystonia 65 0.074
119
ALN001 Aland Island Eye Disease 45 0.074
120
HSH003 Hashimoto Thyroiditis 62 0.074
121
BRN002 Bronchiolitis 56 0.074
122
CCN002 Cocaine Abuse 48 0.073
123
HMT018 Hematopoietic Stem Cell Transplantation 41 0.072
124
P PLM036 Pulmonary Fibrosis 71 0.072
125
PRC012 Pericardial Effusion 51 0.072
126
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.072
127
AND005 Androgen Insensitivity Syndrome, Mild 16 0.071
128
P CLR023 Colorectal Cancer 97 0.071
129
P LCH002 Lichen Planus 53 0.071
130
c HMP029 Hemophilia a 63 0.070
131
P APL001 Aplastic Anemia 75 0.069
132
P CLC005 Celiac Disease 68 0.069
133
MXD005 Mixed Connective Tissue Disease 62 0.069
134
P PRM006 Primary Biliary Cirrhosis 51 0.069
135
P HYP098 Hypereosinophilic Syndrome 63 0.068
136
BRN012 Bronchiolitis Obliterans 58 0.068
137
STS002 Situs Inversus 46 0.068
138
VND001 Vein Disease 47 0.067
139
P NRV006 Nervous System Cancer 60 0.067
140
c CRN177 Coronary Heart Disease 7 20 0.067
141
SKN023 Skin Tag 44 0.066
142
P AMY004 Amyloidosis 65 0.066
143
CHR063 Chronic Mucocutaneous Candidiasis 63 0.066
144
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.066
145
P INF032 Infertility 59 0.066
146
NRT004 Neuritis 52 0.064
147
c ATM010 Autoimmune Hemolytic Anemia 61 0.064
148
GRN017 Granulocytopenia 44 0.064
149
P LPR003 Leprosy 69 0.064
150
PRT029 Parathyroid Adenoma 48 0.063
151
ATM074 Autoimmune Autonomic Ganglionopathy 20 0.063
152
APH002 Aphasia 54 0.063
153
SWL001 Swallowing Disorders 33 0.063
154
LYM021 Lymphadenitis 58 0.063
155
LPR001 Lepromatous Leprosy 50 0.063
156
HNM002 Hinman Syndrome 25 0.063
157
HPT074 Hepatic Adenoma, Somatic 50 0.063
158
OPT009 Optic Neuritis 50 0.062
159
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 41 0.062
160
LKC003 Leukocyte Disease 43 0.061
161
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.061
162
c CRN173 Coronary Heart Disease 8 18 0.061
163
INC022 Inclusion-Cell Disease 46 0.061
164
CRH001 Crohn's Disease 75 0.061
165
c ACT159 Acute Transverse Myelitis 42 0.061
166
P TRC086 Trichohepatoenteric Syndrome 1 48 0.060
167
PLM001 Pulmonary Tuberculosis 67 0.059
168
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.059
169
P FNC043 Fanconi Anemia, Complementation Group E 55 0.059
170
NRF007 Neurofibroma 53 0.058
171
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.058
172
P PLY017 Polyarteritis Nodosa 51 0.058
173
CHR072 Chordoma 61 0.058
174
P GST044 Gastritis 56 0.058
175
ATN004 Autonomic Neuropathy 45 0.058
176
P ABD003 Abdominal Aortic Aneurysm 45 0.058
177
EST005 Esotropia 41 0.058
178
ANS004 Anisometropia 29 0.058
179
THY030 Thyroid Gland Disease 48 0.056
180
THY028 Thyroid Cancer 69 0.054
181
DSS008 Disease of Mental Health 52 0.053
182
SXL003 Sexual Disorder 42 0.053
183
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.052
184
KLN001 Klinefelter's Syndrome 50 0.051
185
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
186
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.051
187
MYC002 Mycobacterium Avium Complex Disease 52 0.050
188
LYM024 Lymphatic System Disease 52 0.049
189
P ATX010 Ataxia Neuropathy Spectrum 30 0.049
190
P TRM003 Tremor 54 0.048
191
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.048
192
CNT098 Central Core Disease 65 0.048
193
MLT021 Multiple System Atrophy 70 0.045
194
P PRK057 Parkinson Disease, Late-Onset 70 0.045
195
c ESS001 Essential Tremor 59 0.045
196
DMN031 Dementia, Lewy Body 58 0.045
197
P SPR098 Supranuclear Palsy, Progressive 56 0.045
198
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.045
199
c PRK059 Parkinson Disease 8 48 0.045
200
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.045
201
LYM116 Lymph Node Disease 47 0.045
202
RMS001 Rem Sleep Behavior Disorder 41 0.045
203
SYN058 Synucleinopathy 38 0.045
204
c PRK025 Parkinson Disease 10 38 0.045
205
c ERL047 Early-Onset Parkinson Disease 34 0.045
206
P PRK073 Parkinson Disease Susceptibility 28 0.045
207
c SNC002 Snca-Related Parkinson Disease 27 0.045
208
PST027 Postencephalitic Parkinson Disease 26 0.045
209
c HRD173 Hereditary Late-Onset Parkinson Disease 24 0.045