Search results for fgfr1

382 hits were found for fgfr1

# Family MCID Name MIFTS Score
1
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 27 9.133
2
P 8P1002 8p11 Myeloproliferative Syndrome 39 8.823
3
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 29 8.680
4
MYL062 Myeloid and Lymphoid Neoplasms Associated with Fgfr1 Abnormalities 26 7.816
5
PFF001 Pfeiffer Syndrome 79 5.333
6
OST044 Osteoglophonic Dysplasia 55 5.039
7
c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 37 4.619
8
P CRN037 Craniosynostosis 68 3.957
9
P TRG016 Trigonocephaly 1 31 3.924
10
HRT030 Hartsfield Syndrome 44 3.894
11
JCK001 Jackson-Weiss Syndrome 51 3.807
12
ENC010 Encephalocraniocutaneous Lipomatosis 46 3.620
13
P BRS047 Breast Cancer 97 3.549
14
P KLL001 Kallmann Syndrome 61 3.545
15
P LNG032 Lung Cancer 98 3.533
16
P HYP730 Hypogonadotropic Hypogonadism 52 3.271
17
P AST007 Astrocytoma 51 3.197
18
P HPT023 Hepatocellular Carcinoma 100 3.087
19
P LKM002 Leukemia 68 3.076
20
P PRS040 Prostate Cancer 97 3.052
21
HYP080 Hypogonadism 50 3.042
22
P HLP001 Holoprosencephaly 67 2.885
23
P ADN016 Adenocarcinoma 64 2.885
24
MYL076 Myeloid/lymphoid Neoplasms Associated with Eosinophilia and Abnormality of Pdgfra, Pdgfrb or Fgfr1 4 2.860
25
P NRB001 Neuroblastoma 72 2.822
26
P GST053 Gastric Cancer 83 2.810
27
P LYM118 Lymphoma 68 2.797
28
P HYP098 Hypereosinophilic Syndrome 67 2.687
29
CLF001 Cleft Lip 53 2.597
30
P BLD134 Bladder Cancer 79 2.502
31
P PNC035 Pancreatic Cancer 84 2.487
32
P GLM045 Glioma 63 2.487
33
P LPM005 Lipomatosis 46 2.471
34
P MLN008 Melanoma 69 2.454
35
END057 Endometrial Cancer 74 2.435
36
MYL031 Myeloproliferative Neoplasm 66 2.413
37
LYM040 Lymphoblastic Lymphoma 54 2.293
38
GLB015 Glioblastoma Multiforme 75 2.283
39
P MDL005 Medulloblastoma 77 2.272
40
GST040 Gastric Adenocarcinoma 70 2.225
41
CLF027 Cleft Palate, Isolated 64 2.225
42
c SYS004 Systemic Mastocytosis 63 2.212
43
SML028 Semilobar Holoprosencephaly 44 2.183
44
ESP021 Esophageal Cancer 90 2.150
45
P OVR042 Ovarian Cancer 88 2.150
46
P NSP012 Nasopharyngeal Carcinoma 66 2.150
47
TTH002 Tooth Agenesis 60 2.150
48
SYN005 Synostosis 45 2.150
49
P ALZ034 Alzheimer Disease 88 2.130
50
EWN003 Ewing Sarcoma 69 2.130
51
SRC014 Sarcoma 65 2.130
52
P SNS001 Sensorineural Hearing Loss 60 2.130
53
P SLV026 Salivary Gland Carcinoma 57 2.130
54
PNC129 Pancreatic Adenocarcinoma 68 2.108
55
HYP042 Hypochondroplasia 60 2.108
56
ANT003 Antley-Bixler Syndrome 47 2.108
57
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 2.013
58
P GLM040 Glioma Susceptibility 1 81 1.922
59
CLF004 Cleft Lip/palate 54 1.900
60
LNG039 Lung Squamous Cell Carcinoma 66 1.851
61
P BRN035 Brain Stem Glioma 52 1.851
62
c LKM063 Leukemia, Chronic Myeloid 72 1.837
63
RST024 Rosette-Forming Glioneuronal Tumor 30 1.837
64
P MST009 Mastocytosis 64 1.822
65
BLD131 Bladder Urothelial Carcinoma 62 1.822
66
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 1.822
67
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.806
68
CSY001 C Syndrome 58 1.806
69
HYP017 Hypophosphatemia 50 1.806
70
P SPL061 Split Hand-Foot Malformation 40 1.806
71
CRZ001 Crouzon Syndrome 68 1.788
72
HMT002 Hematologic Cancer 62 1.788
73
c LRG001 Large Cell Carcinoma 50 1.788
74
MCR173 Microform Holoprosencephaly 44 1.788
75
LBR025 Lobar Holoprosencephaly 43 1.788
76
APR006 Apert Syndrome 70 1.769
77
FBR086 Fibrolamellar Carcinoma 61 1.769
78
ATY042 Atypical Chronic Myeloid Leukemia 49 1.769
79
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 1.769
80
PLM021 Pilomyxoid Astrocytoma 43 1.769
81
MXD050 Mixed Phenotype Acute Leukemia 43 1.769
82
MYL005 Myelofibrosis 70 1.747
83
ODN023 Odontochondrodysplasia 68 1.747
84
ACH004 Achondroplasia 66 1.747
85
SPT006 Septooptic Dysplasia 64 1.747
86
MNK003 Muenke Syndrome 59 1.747
87
GLS001 Gliosarcoma 54 1.747
88
ANK001 Ankylosis 51 1.747
89
GNT002 Giant Cell Glioblastoma 50 1.747
90
CHR563 Chronic Eosinophilic Leukemia 48 1.747
91
P OSS001 Ossifying Fibroma 45 1.747
92
MGS001 Megaesophagus 43 1.747
93
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.722
94
BRN028 Brain Cancer 74 1.722
95
LYM143 Lymphoma, Non-Hodgkin, Familial 72 1.722
96
CHR103 Charge Syndrome 67 1.722
97
P OLG002 Oligodendroglioma 67 1.722
98
STH001 Saethre-Chotzen Syndrome 67 1.722
99
P HYD006 Hydrocephalus 66 1.722
100
P CLD001 Cleidocranial Dysplasia 65 1.722
101
P BND020 Bone Disease 59 1.722
102
P LNG035 Lung Large Cell Carcinoma 54 1.722
103
NRM004 Neuroma 51 1.722
104
c BRS049 Breast Carcinoma in Situ 51 1.722
105
SPT005 Spotted Fever 49 1.722
106
P RDL002 Radioulnar Synostosis 45 1.722
107
CHN004 Chondroblastoma 40 1.722
108
c LKM061 Leukemia, Acute Myeloid 84 1.418
109
c NRB010 Neuroblastoma 1 49 1.366
110
P LNG064 Lung Cancer Susceptibility 3 78 1.351
111
CHR619 Chromosome 2q35 Duplication Syndrome 62 1.335
112
c CNG562 Congenital Hypogonadotropic Hypogonadism 34 1.335
113
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 40 1.318
114
P RNL100 Renal Hypodysplasia/aplasia 1 63 1.299
115
DYS006 Dysembryoplastic Neuroepithelial Tumor 38 1.299
116
FGF014 Fgfr Craniosynostosis Syndromes 27 1.299
117
c PRM149 Primary Hypereosinophilic Syndrome 34 1.277
118
SYN106 Syndromic Craniosynostosis 33 1.277
119
MYL060 Myeloid and Lymphoid Neoplasms Associated with Pdgfra Rearrangement 30 1.277
120
ISL084 Isolated Trigonocephaly 21 1.277
121
P THN009 Thanatophoric Dysplasia, Type I 62 1.251
122
SPP011 Suppression of Tumorigenicity 12 59 1.251
123
P RTN008 Retinitis Pigmentosa 79 1.217
124
NVS017 Nevus, Epidermal 68 1.217
125
P PRT008 Proteus Syndrome 64 1.217
126
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 62 1.217
127
LCR014 Lacrimoauriculodentodigital Syndrome 61 1.217
128
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 1.217
129
c LPM012 Lipomatosis, Multiple 60 1.217
130
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 1.217
131
P VND007 Van Der Woude Syndrome 1 58 1.217
132
HMF006 Hemifacial Microsomia 55 1.217
133
OCL039 Oculoectodermal Syndrome 53 1.217
134
CLB010 Coloboma of Macula 52 1.217
135
CHN065 Choanal Atresia, Posterior 49 1.217
136
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 45 1.217
137
HYP059 Hypertelorism, Microtia, Facial Clefting Syndrome 45 1.217
138
P OST028 Osteochondroma 45 1.217
139
P ORF002 Orofacial Cleft 44 1.217
140
DYS018 Dysostosis 44 1.217
141
c HYP763 Hypogonadotropic Hypogonadism 23 Without Anosmia 43 1.217
142
SKN023 Skin Tag 42 1.217
143
SYN031 Synovial Chondromatosis 42 1.217
144
PLG004 Plagiocephaly 41 1.217
145
PHS001 Phosphorus Metabolism Disease 40 1.217
146
CRP003 Corpus Callosum Lipoma 34 1.217
147
c ADL008 Adult Oligodendroglioma 34 1.217
148
P BND014 Bone Development Disease 33 1.217
149
c CTR185 Cataract 30 32 1.217
150
CHL006 Childhood Oligodendroglioma 31 1.217
151
SPN007 Spinal Cord Oligodendroglioma 30 1.217
152
CRB034 Cerebral Hemisphere Lipoma 26 1.217
153
SPN004 Spinal Cord Lipoma 23 1.217
154
CNT024 Central Nervous System Lipoma 21 1.217
155
c SML038 Small Cell Cancer of the Lung 65 0.199
156
SQM006 Squamous Cell Carcinoma 60 0.163
157
P MYL006 Myeloid Leukemia 60 0.122
158
JVN009 Juvenile Pilocytic Astrocytoma 55 0.122
159
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.115
160
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.115
161
c SPL067 Split-Hand/foot Malformation 1 46 0.108
162
OST159 Osteogenic Sarcoma 66 0.091
163
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.081
164
c ACT073 Acute Leukemia 58 0.081
165
PLY150 Polykaryocytosis Inducer 31 0.081
166
SPN186 Spinal Cord Injury 60 0.070
167
DCT002 Ductal Carcinoma in Situ 59 0.070
168
P DBT005 Diabetes Insipidus 55 0.070
169
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.070
170
P INS002 in Situ Carcinoma 53 0.070
171
OST011 Osteomalacia 52 0.070
172
PRS129 Prostatic Hyperplasia, Benign 49 0.070
173
GLL048 Glial Tumor 45 0.070
174
ORL015 Oral Squamous Cell Carcinoma 43 0.070
175
OVR094 Ovarian Epithelial Cancer 38 0.070
176
GST019 Gastrointestinal Stromal Tumor 78 0.058
177
P PHC003 Pheochromocytoma 71 0.058
178
P ESS003 Essential Thrombocythemia 68 0.058
179
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.058
180
P ANR048 Aniridia 1 63 0.058
181
ANR007 Anorexia Nervosa 63 0.058
182
c BRN108 Branchiootic Syndrome 1 62 0.058
183
P TRC086 Trichohepatoenteric Syndrome 1 62 0.058
184
ACN002 Acanthosis Nigricans 60 0.058
185
ADN018 Adenoma 59 0.058
186
P PLY018 Polycythemia 56 0.058
187
P CHN012 Chondrosarcoma 56 0.058
188
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.058
189
PRS045 Prostatic Hypertrophy 53 0.058
190
DMY004 Demyelinating Disease 52 0.058
191
PRS021 Prostatic Adenoma 51 0.058
192
LNG031 Lung Benign Neoplasm 51 0.058
193
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.058
194
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.058
195
P OVR082 Overgrowth Syndrome 50 0.058
196
GYN001 Gynecomastia 49 0.058
197
BRN071 Brain Injury 49 0.058
198
HYP025 Hyperphosphatemia 48 0.058
199
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.058
200
ADR040 Adrenal Gland Pheochromocytoma 46 0.058
201
c HYP513 Hypogonadotropic Hypogonadism 1 with or Without Anosmia 45 0.058
202
DWR001 Dwarfism 44 0.058
203
ONC003 Oncogenic Osteomalacia 42 0.058
204
P RRT020 Rare Tumor 41 0.058
205
CHR178 Chromosomal Triplication 35 0.058
206
ATX010 Ataxia Neuropathy Spectrum 34 0.058
207
ACT064 Acute Necrotizing Encephalitis 33 0.058
208
INF021 Infant Gynecomastia 31 0.058
209
BLD137 Blood Group--Ahonen 16 0.058
210
P CLR023 Colorectal Cancer 99 0.041
211
NRL016 Neural Tube Defects 82 0.041
212
OST012 Osteoarthritis 78 0.041
213
P OST002 Osteoporosis 74 0.041
214
SVR004 Severe Combined Immunodeficiency 73 0.041
215
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.041
216
P RTN024 Retinoblastoma 73 0.041
217
P EPL164 Epilepsy 71 0.041
218
P SRC025 Sarcoidosis 1 70 0.041
219
MYL009 Myelodysplastic Syndrome 70 0.041
220
DWN001 Down Syndrome 70 0.041
221
ADN011 Adenoid Cystic Carcinoma 70 0.041
222
PLY001 Polycythemia Vera 69 0.041
223
P LKM062 Leukemia, Acute Lymphoblastic 69 0.041
224
P LVR013 Liver Disease 68 0.041
225
CST001 Costello Syndrome 68 0.041
226
RCK004 Rickets 68 0.041
227
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.041
228
P THR014 Thrombocytopenia 67 0.041
229
PRT010 Parathyroid Carcinoma 67 0.041
230
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.041
231
AND002 Androgen Insensitivity Syndrome 66 0.041
232
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.041
233
P LPS002 Liposarcoma 65 0.041
234
DRM014 Dermatofibrosarcoma Protuberans 65 0.041
235
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.041
236
CLN015 Colon Adenocarcinoma 65 0.041
237
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.041
238
DSM004 Desmoid Tumor 64 0.041
239
P RHB003 Rhabdomyosarcoma 63 0.041
240
P HYP069 Hyperparathyroidism 63 0.041
241
P LMY004 Leiomyosarcoma 63 0.041
242
RHB001 Rhabdoid Cancer 63 0.041
243
c OPT053 Optic Atrophy 1 63 0.041
244
HYP810 Hypereosinophilic Syndrome, Idiopathic 62 0.041
245
FTT001 Fatty Liver Disease 61 0.041
246
RTN017 Retinal Detachment 61 0.041
247
DPH001 Diphtheria 60 0.041
248
P BNG030 Benign Ependymoma 60 0.041
249
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.041
250
P AXN002 Axenfeld-Rieger Syndrome 59 0.041
251
P ERY058 Erythrocytosis, Familial, 1 59 0.041
252
c SVR003 Severe Congenital Neutropenia 59 0.041
253
ALP097 Alopecia Universalis Congenita 59 0.041
254
P MLT007 Multiple Epiphyseal Dysplasia 58 0.041
255
CHR072 Chordoma 58 0.041
256
c CHR417 Chronic Graft Versus Host Disease 57 0.041
257
HYP266 Hypoxia 57 0.041
258
P BPL003 Bipolar Disorder 56 0.041
259
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.041
260
SFT003 Soft Tissue Sarcoma 56 0.041
261
PPL025 Popliteal Pterygium Syndrome 56 0.041
262
BRN004 Brain Edema 56 0.041
263
P PLM034 Pulmonary Emphysema 55 0.041
264
CHR100 Chronic Ulcer of Skin 55 0.041
265
P SCL048 Sclerosteosis 55 0.041
266
HRY003 Hairy Cell Leukemia 55 0.041
267
CLL010 Cellular Ependymoma 54 0.041
268
AMN001 Amenorrhea 54 0.041
269
CLL003 Cellulitis 54 0.041
270
P BRC006 Brachydactyly 53 0.041
271
CLR030 Clear Cell Renal Cell Carcinoma 53 0.041
272
TRC023 Trichinosis 53 0.041
273
P HYP083 Hypopituitarism 53 0.041
274
SPN035 Spindle Cell Sarcoma 53 0.041
275
c FML008 Familial Retinoblastoma 53 0.041
276
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.041
277
c BRL011 Bare Lymphocyte Syndrome, Type I 52 0.041
278
NTR018 Neutrophilia, Hereditary 52 0.041
279
TRM010 Traumatic Brain Injury 51 0.041
280
BLL003 Bell's Palsy 51 0.041
281
FBR008 Fibrillary Astrocytoma 51 0.041
282
P HYP040 Hypospadias 51 0.041
283
STR008 Strongyloidiasis 51 0.041
284
PRT029 Parathyroid Adenoma 50 0.041
285
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.041
286
ONC007 Oncocytoma 49 0.041
287
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.041
288
P CRV039 Cervicitis 49 0.041
289
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.041
290
END021 Endomyocardial Fibrosis 49 0.041
291
AGG002 Aggressive Systemic Mastocytosis 49 0.041
292
ACT029 Acute Interstitial Pneumonia 49 0.041
293
QDR001 Quadriplegia 48 0.041
294
IMM105 Immunodeficiency with Hyper-Igm, Type 3 48 0.041
295
CLC006 Calcinosis 48 0.041
296
CLF056 Cleft Lip with or Without Cleft Palate 47 0.041
297
AML029 Ameloblastoma 46 0.041
298
CNT019 Central Neurocytoma 46 0.041
299
P BNG032 Benign Mesothelioma 46 0.041
300
c MLG068 Malignant Glioma 46 0.041
301
EPD015 Epidemic Typhus 45 0.041
302
c THN010 Thanatophoric Dysplasia, Type Ii 45 0.041
303
c RTN150 Retinitis Pigmentosa 10 45 0.041
304
P DCR003 Dacryoadenitis 45 0.041
305
P DSR089 Disorders of Sexual Development 45 0.041
306
SPS057 Spasticity 45 0.041
307
CHL149 Childhood Acute Myeloid Leukemia 44 0.041
308
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.041
309
ESP018 Esophageal Candidiasis 44 0.041
310
c NNN011 Noonan Syndrome 4 44 0.041
311
c ATM097 Autoimmune Lymphoproliferative Syndrome, Type Iia 43 0.041
312
P HYP078 Hypertrophy of Breast 43 0.041
313
BNM001 Bone Marrow Cancer 43 0.041
314
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.041
315
VRL003 Variola Major 42 0.041
316
MST004 Mast Cell Neoplasm 42 0.041
317
P WST004 West Nile Encephalitis 42 0.041
318
c MLG079 Malignant Pleural Mesothelioma 42 0.041
319
MYF002 Myofascial Pain Syndrome 42 0.041
320
MSN004 Mesenchymal Cell Neoplasm 41 0.041
321
c CRD079 Cardiomyopathy, Familial Hypertrophic, 9 41 0.041
322
MTL005 Metal Allergy 41 0.041
323
c MJR024 Major Affective Disorder 9 41 0.041
324
PCD001 Pica Disease 41 0.041
325
SKN006 Skin Sarcoidosis 41 0.041
326
LRG008 Large Granular Lymphocyte Leukemia 41 0.041
327
c SCN006 Secondary Syphilis 40 0.041
328
c 46X055 46,xy Sex Reversal 3 40 0.041
329
WST003 West Nile Fever 40 0.041
330
MNK002 Monkeypox 39 0.041
331
SPS004 Spastic Quadriplegia 39 0.041
332
FRM003 Farmer's Lung 39 0.041
333
c HYP507 Hypotrichosis 1 39 0.041
334
ADN067 Adenoid Hypertrophy 39 0.041
335
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.041
336
PRP005 Parapsoriasis 38 0.041
337
c MJR022 Major Affective Disorder 8 38 0.041
338
CRB009 Cerebritis 37 0.041
339
ORL019 Oral Hairy Leukoplakia 37 0.041
340
c RTN130 Retinitis Pigmentosa 46 37 0.041
341
NRW001 Norwegian Scabies 37 0.041
342
NRS005 Neurosarcoidosis 36 0.041
343
PLN026 Pilonidal Sinus 35 0.041
344
GLN002 Glanders 35 0.041
345
ADN064 Adenohypophysitis 35 0.041
346
NCK004 Nickel Allergic Contact Dermatitis 35 0.041
347
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.041
348
FCL090 Facial Cleft 34 0.041
349
SBC019 Subcutaneous Mycosis 34 0.041
350
PPL052 Papillomatosis, Confluent and Reticulated 33 0.041
351
ALR002 Al-Raqad Syndrome 33 0.041
352
TRT003 Tertiary Syphilis 33 0.041
353
GRN009 Granulomatous Hepatitis 33 0.041
354
P MYX008 Myxoid Chondrosarcoma 32 0.041
355
GLB024 Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor 32 0.041
356
BRD003 Bird Fancier's Lung 32 0.041
357
c INV003 Invasive Malignant Thymoma 32 0.041
358
FLL019 Follicular Mucinosis 31 0.041
359
SPN011 Spongiotic Dermatitis 31 0.041
360
c DBT053 Diabetes Mellitus, Insulin-Dependent, 23 31 0.041
361
PRT031 Parotid Disease 30 0.041
362
c CNG608 Congenital Hypopituitarism 30 0.041
363
c ERL004 Early Yaws 30 0.041
364
ACT022 Acute Retinal Necrosis Syndrome 30 0.041
365
JK3001 Jak3-Deficient Severe Combined Immunodeficiency 29 0.041
366
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.041
367
c VRL008 Viral Exanthem 28 0.041
368
CRK001 Cork-Handlers' Disease 27 0.041
369
c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 27 0.041
370
DFF007 Diffuse Infiltrative Lymphocytosis Syndrome 27 0.041
371
DSS003 Disseminated Eosinophilic Collagen Disease 25 0.041
372
CMP097 Complex Chromosomal Rearrangement 25 0.041
373
c HYP444 Hypogonadotropic Hypogonadism 9 with or Without Anosmia 24 0.041
374
EXT044 Extraventricular Neurocytoma 22 0.041
375
PPL060 Papillary Glioneuronal Tumors 21 0.041
376
VNT001 Ventilation Pneumonitis 21 0.041
377
GLB014 Glioblastoma Neural Subtype 20 0.041
378
c NNS019 Nonsyndromic Holoprosencephaly 16 0.041
379
MYL079 Myeloid and Lymphoid Neoplasms Associated with Pdgfrb Rearrangement 14 0.041
382
ISL139 Isolated Congenital Hypogonadotropic Hypogonadism 10 0.041
Content
Loading form....