Search results for "germinoma"

The MalaCard for "germinoma" has been retired.
Searching MalaCards for entries containing "germinoma"

290 hits were found for 'germinoma'

# Family MCID Name MIFTS Score
1
P CNT037 Central Nervous System Germinoma 33 7.182
2
BRN031 Brain Germinoma 29 5.478
3
PNL011 Pineal Region Germinoma 18 3.916
4
c ADL036 Adult Central Nervous System Germinoma 17 3.874
5
CHL051 Childhood Brain Germinoma 14 3.857
6
CHL027 Childhood Central Nervous System Germinoma 13 3.163
7
MLG078 Malignant Pineal Area Germ Cell Neoplasm 23 3.142
8
EXT055 Extragonadal Germinoma 11 2.281
9
CRB009 Cerebritis 38 0.143
10
P DBT005 Diabetes Insipidus 53 0.138
11
P TRT010 Teratoma 52 0.138
12
SMN007 Seminoma 42 0.121
13
MDS022 Mediastinitis 41 0.121
14
P PRC019 Precocious Puberty 51 0.101
15
P CRV039 Cervicitis 44 0.094
16
TST043 Testicular Seminoma 40 0.094
17
LYM043 Lymphocytic Hypophysitis 31 0.094
18
KLN001 Klinefelter's Syndrome 55 0.085
19
PRT036 Peritonitis 62 0.076
20
P HYP083 Hypopituitarism 52 0.076
21
MXD032 Mixed Germ Cell Tumor 31 0.076
22
P MDL005 Medulloblastoma 77 0.066
23
P AST007 Astrocytoma 65 0.066
24
P MNN013 Meningitis 65 0.066
25
P GLM045 Glioma 58 0.066
26
EMB004 Embryonal Carcinoma 56 0.066
27
MTR010 Mature Teratoma 42 0.066
28
P HYD006 Hydrocephalus 67 0.054
29
OBS002 Obsessive-Compulsive Disorder 66 0.054
30
c HMP029 Hemophilia a 64 0.054
31
VNW001 Von Willebrand's Disease 61 0.054
32
FCT006 Factor V Deficiency 60 0.054
33
P THR015 Thrombophilia 59 0.054
34
P ANT006 Antiphospholipid Syndrome 58 0.054
35
HYP020 Hyperprolactinemia 57 0.054
36
P HMR003 Hemorrhagic Disease 57 0.054
37
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.054
38
c THR092 Thrombophilia Due to Thrombin Defect 56 0.054
39
P BDD001 Budd-Chiari Syndrome 56 0.054
40
P AGN002 Agnosia 56 0.054
41
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 0.054
42
P HYP620 Hypoprothrombinemia 54 0.054
43
PRT014 Protein S Deficiency 52 0.054
44
DSS009 Disseminated Intravascular Coagulation 51 0.054
45
RTN023 Retinitis 49 0.054
46
PRT018 Portal Vein Thrombosis 49 0.054
47
ANT024 Anthrax Disease 48 0.054
48
CHR074 Choriocarcinoma 46 0.054
49
P AFB001 Afibrinogenemia 46 0.054
50
P CRN035 Cranial Nerve Palsy 43 0.054
51
NRN002 Neuronitis 42 0.054
52
PRP028 Peripheral Vertigo 41 0.054
53
P CHR342 Chiari Malformation 37 0.054
54
CTN013 Cutaneous Anthrax 35 0.054
55
CRB132 Cerebral Sinovenous Thrombosis 31 0.054
56
PRS120 Persistent Idiopathic Facial Pain 21 0.054
57
ADT001 Auditory Agnosia 21 0.054
58
HPT023 Hepatocellular Carcinoma 91 0.038
59
ADN021 Adenomatous Polyposis Coli 76 0.038
60
P ART022 Arthritis 75 0.038
61
TST021 Testicular Germ Cell Tumor 70 0.038
62
P LYM118 Lymphoma 70 0.038
63
P KRB001 Krabbe Disease 69 0.038
64
SMT004 Smith-Lemli-Opitz Syndrome 67 0.038
65
SRC014 Sarcoma 66 0.038
66
P GLB002 Glioblastoma 66 0.038
67
DWN001 Down Syndrome 65 0.038
68
P DYS154 Dystonia 64 0.038
69
GLN010 Glanzmann Thrombasthenia 63 0.038
70
P ANR007 Anorexia Nervosa 63 0.038
71
CRD119 Cardiac Arrest 63 0.038
72
c HMP004 Hemophilia B 62 0.038
73
FCT003 Factor X Deficiency 62 0.038
74
FCT007 Factor Vii Deficiency 62 0.038
75
P MYM002 Moyamoya Disease 60 0.038
76
PLM033 Pulmonary Embolism 59 0.038
77
P ENC018 Encephalopathy 59 0.038
78
c HPT003 Hepatitis a 59 0.038
79
ADN018 Adenoma 59 0.038
80
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 0.038
81
FLL027 Fallopian Tube Carcinoma 58 0.038
82
ANR040 Aneurysm 57 0.038
83
c ACT210 Acute Respiratory Distress Syndrome 57 0.038
84
LGG001 Legg-Calve-Perthes Disease 57 0.038
85
CHL067 Cholecystitis 56 0.038
86
TRN015 Transient Cerebral Ischemia 56 0.038
87
P HMP007 Hemophilia 56 0.038
88
DMY004 Demyelinating Disease 55 0.038
89
CHR029 Choroid Plexus Papilloma 55 0.038
90
PTT006 Pituitary Adenoma 55 0.038
91
PPL022 Papilloma 55 0.038
92
P TRM003 Tremor 54 0.038
93
P INT030 Intracranial Aneurysm 54 0.038
94
c AFB002 Afibrinogenemia, Congenital 54 0.038
95
P EPN002 Ependymoma 53 0.038
96
P ATX004 Ataxia 53 0.038
97
ESP023 Esophageal Disease 53 0.038
98
INT075 Intracranial Hypertension 53 0.038
99
P CNT005 Central Nervous System Lymphoma 53 0.038
100
P GND004 Gonadal Dysgenesis 53 0.038
101
TST014 Testicular Cancer 52 0.038
102
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 52 0.038
103
THR016 Thrombophlebitis 52 0.038
104
UTR024 Uterine Carcinosarcoma 52 0.038
105
CHC001 Chickenpox 52 0.038
106
VND001 Vein Disease 52 0.038
107
PRT011 Protein C Deficiency 51 0.038
108
HNT002 Hantavirus Pulmonary Syndrome 51 0.038
109
MRK001 Merkel Cell Carcinoma 51 0.038
110
AMN001 Amenorrhea 51 0.038
111
FML037 Female Breast Cancer 51 0.038
112
FCT004 Factor Xii Deficiency 51 0.038
113
c MLG068 Malignant Glioma 50 0.038
114
FCL012 Facial Paralysis 50 0.038
115
PLC005 Placental Insufficiency 50 0.038
116
UTR033 Uterine Corpus Cancer 50 0.038
117
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.038
118
VNW005 Von Willebrand Disease, Type 1 50 0.038
119
PST095 Post-Thrombotic Syndrome 50 0.038
120
GNG004 Ganglioglioma 49 0.038
121
PLM032 Pulmonary Blastoma 49 0.038
122
ACN001 Acinar Cell Carcinoma 48 0.038
123
P CMP008 Compartment Syndrome 48 0.038
124
PPL021 Papilledema 48 0.038
125
MYL001 Myelitis 48 0.038
126
SPR010 Sporotrichosis 48 0.038
127
SPL012 Splenic Disease 47 0.038
128
P OTT001 Otitis Externa 47 0.038
129
SYN036 Syncope 47 0.038
130
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.038
131
PLC007 Placental Abruption 47 0.038
132
P AMY060 Amyloidosis, Primary Localized Cutaneous, 1 47 0.038
133
PRM020 Premenstrual Tension 46 0.038
134
c CHR086 Chronic Conjunctivitis 46 0.038
135
PRS039 Prostate Adenocarcinoma 46 0.038
136
TBR011 Tuberculous Meningitis 46 0.038
137
INT017 Intestinal Schistosomiasis 46 0.038
138
HML015 Hemolytic Anemia Due to Triosephosphate Isomerase Deficiency 46 0.038
139
PHH001 Phaeohyphomycosis 46 0.038
140
P ANL018 Analbuminemia 46 0.038
141
c SVR056 Severe Hemophilia a 46 0.038
142
P BLD051 Blood Coagulation Disease 45 0.038
143
TST015 Testicular Disease 45 0.038
144
SGN002 Signet Ring Cell Adenocarcinoma 45 0.038
145
P ATR005 Atrophic Gastritis 45 0.038
146
PPL007 Papillary Serous Adenocarcinoma 44 0.038
147
CLL001 Cellular Schwannoma 44 0.038
148
SPN021 Spinal Meningioma 44 0.038
149
RYN001 Raynaud Disease 44 0.038
150
CHR008 Choroiditis 43 0.038
151
CRT015 Carotid Artery Occlusion 43 0.038
152
DRM013 Dermoid Cyst 43 0.038
153
PLM020 Pleomorphic Xanthoastrocytoma 43 0.038
154
P RTN014 Retinal Artery Occlusion 43 0.038
155
GST052 Gestational Choriocarcinoma 43 0.038
156
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 43 0.038
157
c MLG064 Malignant Ependymoma 42 0.038
158
MLR002 Miliary Tuberculosis 42 0.038
159
c LNG098 Long Qt Syndrome 14 42 0.038
160
c LNG096 Long Qt Syndrome 15 42 0.038
161
TBL003 Tubular Adenocarcinoma 42 0.038
162
P PRP034 Purpura Fulminans 42 0.038
163
ESN004 Eosinophilic Gastritis 42 0.038
164
CDQ001 Cauda Equina Syndrome 42 0.038
165
c ACQ014 Acquired Hemophilia 42 0.038
166
TLR001 Tularemia 42 0.038
167
FCT005 Factor Xiii Deficiency 42 0.038
168
THR035 Thrombasthenia 42 0.038
169
NCR004 Nocardiosis 42 0.038
170
GST078 Gastrointestinal Allergy 41 0.038
171
P DYS026 Dysfibrinogenemia 41 0.038
172
SQM002 Squamous Cell Papilloma 41 0.038
173
EXT056 External Ear Disease 41 0.038
174
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.038
175
BSL006 Basaloid Squamous Cell Carcinoma 41 0.038
176
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 0.038
177
SCL017 Sclerosing Hemangioma 41 0.038
178
PRM026 Primary Systemic Mycosis 41 0.038
179
ISC015 Ischemic Colitis 40 0.038
180
INT040 Intrinsic Asthma 40 0.038
181
SWT002 Sweat Gland Cancer 40 0.038
182
OPT008 Optic Nerve Neoplasm 40 0.038
183
CYS009 Cystadenoma 40 0.038
184
c SML034 Small Cell Neuroendocrine Carcinoma 40 0.038
185
KRN001 Korean Hemorrhagic Fever 40 0.038
186
P CNT036 Central Nervous System Germ Cell Tumor 39 0.038
187
BRS090 Breast Reconstruction 39 0.038
188
c INH004 Inherited Blood Coagulation Disease 39 0.038
189
INH001 Inhalation Anthrax 39 0.038
190
c ACQ042 Acquired Hemophilia a 39 0.038
191
GRM001 Germ Cell and Embryonal Cancer 39 0.038
192
VRT003 Vertebrobasilar Insufficiency 39 0.038
193
BRN026 Branch Retinal Artery Occlusion 39 0.038
194
AGR018 Agraphia 39 0.038
195
LYM002 Lymphoplasmacyte-Rich Meningioma 39 0.038
196
MNN021 Meningococcemia 38 0.038
197
P TRC005 Tracheal Stenosis 38 0.038
198
FCL011 Facial Nerve Disease 38 0.038
199
BRT043 Bartonellosis 38 0.038
200
MCR019 Microglandular Adenosis 38 0.038
201
SPN033 Spontaneous Ocular Nystagmus 38 0.038
202
OTM001 Otomycosis 37 0.038
203
SHW001 Shwartzman Phenomenon 37 0.038
204
RDT001 Radiation Cystitis 37 0.038
205
FRY001 Frey Syndrome 37 0.038
206
CRV036 Cervical Carcinosarcoma 37 0.038
207
GRN022 Granulosa Cell Tumor of the Ovary 37 0.038
208
P CLR001 Clear Cell Acanthoma 37 0.038
209
LCH001 Leech Infestation 37 0.038
210
VRT001 Vertebral Artery Occlusion 37 0.038
211
CHN002 Chancroid 36 0.038
212
SPN185 Spinal Cord Infarction 36 0.038
213
FCL049 Focal Hand Dystonia 36 0.038
214
INT082 Intraocular Retinoblastoma 36 0.038
215
P MXD016 Mixed Gonadal Dysgenesis 36 0.038
216
PLM016 Pleomorphic Carcinoma 36 0.038
217
FML005 Female Reproductive Endometrioid Cancer 36 0.038
218
BRS032 Breast Papillary Carcinoma 35 0.038
219
CRB038 Cerebral Ventricle Cancer 35 0.038
220
DYS006 Dysembryoplastic Neuroepithelial Tumor 35 0.038
221
BLT003 Blue Toe Syndrome 35 0.038
222
WLL004 Wallerian Degeneration 35 0.038
223
CRB029 Cerebellopontine Angle Tumor 35 0.038
224
c NRV012 Nervous System Benign Neoplasm 35 0.038
225
TRC026 Tracheal Disease 35 0.038
226
FMR003 Femoral Neuropathy 34 0.038
227
c BRS046 Breast Benign Neoplasm 34 0.038
228
PRG092 Pregnancy Loss, Recurrent 1 34 0.038
229
MSN003 Mesenteric Vascular Occlusion 34 0.038
230
FRN014 Fournier Gangrene 34 0.038
231
ORC001 Orchitis 34 0.038
232
CLR018 Clear Cell Meningioma 33 0.038
233
SGT001 Sagittal Sinus Thrombosis 33 0.038
234
SBN001 Subendocardial Myocardial Infarction 33 0.038
235
DYS013 Dysbaric Osteonecrosis 33 0.038
236
GNT005 Giant Hemangioma 33 0.038
237
c ACT037 Acute Dacryocystitis 33 0.038
238
QLT001 Qualitative Platelet Defect 32 0.038
239
FCT016 Factor V and Factor Viii, Combined Deficiency of 32 0.038
240
PNC018 Pancreatic Serous Cystadenoma 32 0.038
241
MRN001 Marantic Endocarditis 32 0.038
242
THR011 Thoracic Benign Neoplasm 32 0.038
243
P CRB059 Cerebellar Degeneration 32 0.038
244
MXD026 Mixed Glioma 32 0.038
245
P BNG002 Benign Meningioma 32 0.038
246
LVD002 Livedoid Vasculopathy 31 0.038
247
INT050 Intestinal Impaction 31 0.038
248
ECH002 Echolalia 31 0.038
249
ACN019 Acanthamoeba Keratitis 31 0.038
250
CCL002 Cecal Disease 31 0.038
251
LWR004 Lower Urinary Tract Calculus 31 0.038
252
MLG007 Malignant Skin Fibrous Histiocytoma 31 0.038
253
P FRT001 Fourth Cranial Nerve Palsy 31 0.038
254
PLY021 Polyradiculopathy 30 0.038
255
SKL005 Skull Base Meningioma 30 0.038
256
PRL005 Proliferative Fasciitis 30 0.038
257
CHR033 Chordoid Glioma 30 0.038
258
c MLG063 Malignant Dermis Tumor 29 0.038
259
PRN032 Paraneoplastic Cerebellar Degeneration 29 0.038
260
ANT013 Anterior Spinal Artery Syndrome 29 0.038
261
LNG009 Lung Meningioma 28 0.038
262
c BRS007 Breast Malignant Phyllodes Tumor 28 0.038
263
TRG001 Trigonitis 27 0.038
264
ANT022 Anterior Cranial Fossa Meningioma 26 0.038
265
TNY001 Tanycytic Ependymoma 26 0.038
266
VSL003 Visual Agnosia 26 0.038
267
END018 Endometrium Carcinoma in Situ 26 0.038
268
OCC005 Occlusion Precerebral Artery 25 0.038
269
c MNS008 Monosomy 21 25 0.038
270
OPP001 Opportunistic Bacterial Infectious Disease 25 0.038
271
OLF002 Olfactory Groove Meningioma 25 0.038
272
SPH007 Sphenoid Sinusitis 24 0.038
273
CRB032 Cerebral Convexity Meningioma 24 0.038
274
GLM005 Glomangiosarcoma 24 0.038
275
INT076 Intracranial Sinus Thrombosis 24 0.038
276
SBS002 Substernal Goiter 24 0.038
277
ATY007 Atypical Follicular Adenoma 24 0.038
278
PNM002 Pneumonic Tularemia 23 0.038
279
NRS005 Neurosarcoidosis 23 0.038
280
MYT019 May-Thurner Syndrome 23 0.038
281
P FRM004 Foramen Magnum Meningioma 21 0.038
282
GLS008 Glossopharyngeal Nerve Disease 21 0.038
283
P SPN039 Spinal Canal and Spinal Cord Meningioma 20 0.038
284
HMM001 Hemometra 19 0.038
285
GRW021 Growing Teratoma Syndrome 18 0.038
286
CRB017 Cerebral Falx Meningioma 18 0.038
287
PNL021 Pineal Cyst 17 0.038
288
PTR003 Petrous Apex Meningioma 15 0.038
289
GRN020 Granulomatous Hypophysitis 13 0.038
290
URT015 Urethral False Passage 11 0.038