Search results for "foot and mouth disease"

The MalaCard for "foot and mouth disease" has been retired.
Searching MalaCards for entries containing "foot and mouth disease"

545 hits were found for 'foot and mouth disease'

# Family MCID Name MIFTS Score
1
HND002 Hand, Foot and Mouth Disease 48 4.066
2
MTH009 Mouth Disease 63 0.657
3
BRN106 Burns 52 0.295
4
P NRP001 Neuropathy 60 0.282
5
END072 Endotheliitis 42 0.218
6
P ART022 Arthritis 75 0.213
7
P HPT021 Hepatitis 70 0.211
8
P LKM002 Leukemia 70 0.204
9
P MCR129 Microvascular Complications of Diabetes 1 57 0.202
10
CRB009 Cerebritis 38 0.196
11
P LYM118 Lymphoma 70 0.194
12
FTD001 Foot Drop 32 0.194
13
PRP027 Peripheral Vascular Disease 69 0.179
14
P RHM011 Rheumatoid Arthritis 88 0.175
15
ORL011 Oral Cancer 55 0.165
16
P ORL007 Oral Cavity Cancer 58 0.163
17
P AST005 Asthma 82 0.156
18
P PRD008 Periodontitis 46 0.155
19
c PND001 Pain Disorder 55 0.155
20
P CLR023 Colorectal Cancer 97 0.154
21
SRC014 Sarcoma 66 0.154
22
TTH006 Tooth Disease 52 0.151
23
P ART023 Arthropathy 63 0.144
24
ADM013 Adamantinoma of Long Bones 59 0.143
25
RSP006 Respiratory System Disease 62 0.142
26
ATH003 Atherosclerosis 62 0.140
27
DRM006 Dermatitis 61 0.140
28
NRM005 Neuromuscular Disease 57 0.139
29
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.139
30
P MYP004 Myopathy 67 0.138
31
P ENC004 Encephalitis 61 0.137
32
P PRP019 Peripheral Nervous System Disease 54 0.137
33
SKN016 Skin Disease 68 0.136
34
ADL002 Adult Syndrome 53 0.136
35
NTR005 Nutritional Deficiency Disease 39 0.135
36
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.133
37
MVM001 Movement Disease 54 0.133
38
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.131
39
SPL040 Split Hand 37 0.131
40
TBR010 Tuberculosis 69 0.131
41
P CRV039 Cervicitis 44 0.130
42
P SPS003 Spastic Diplegia 53 0.130
43
PCK002 Pick Disease 67 0.130
44
BRT030 Birth Defects 43 0.129
45
P INF038 Influenza 74 0.128
46
CNN005 Connective Tissue Disease 61 0.128
47
ACR041 Acromelic Frontonasal Dysostosis 46 0.128
48
GLC008 Glucose Metabolism Disease 47 0.127
49
P PNM007 Pneumonia 66 0.127
50
P NRV006 Nervous System Cancer 62 0.123
51
APH001 Aphthous Stomatitis 62 0.123
52
CRH001 Crohn's Disease 76 0.123
53
HYP266 Hypoxia 55 0.122
54
P NRV007 Nervous System Disease 71 0.122
55
BNS002 Bone Structure Disease 36 0.121
56
P CHR345 Chronic Pain 49 0.121
57
P INF032 Infertility 61 0.121
58
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.120
59
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.119
60
PHY002 Physical Disorder 44 0.119
61
PRP021 Peripheral Nervous System Neoplasm 50 0.118
62
c CNT035 Central Nervous System Disease 59 0.118
63
P SCH015 Schizophrenia 76 0.117
64
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.117
65
ATN002 Autonomic Nervous System Disease 47 0.116
66
OCL009 Ocular Cancer 62 0.116
67
P LPS004 Lupus Erythematosus 63 0.116
68
P MSC033 Muscle Disorders 52 0.115
69
LRN003 Learning Disability 51 0.115
70
RHM027 Rheumatic Disease 57 0.115
71
ANR040 Aneurysm 57 0.115
72
GST053 Gastric Cancer 77 0.115
73
BLD053 Blood Platelet Disease 46 0.114
74
MSC004 Muscle Tissue Disease 36 0.114
75
VND001 Vein Disease 52 0.114
76
JNT002 Joint Disorders 56 0.113
77
ALL026 Allergic Hypersensitivity Disease 53 0.113
78
SLP005 Sleep Disorder 53 0.113
79
PRD007 Periodontal Disease 43 0.113
80
CHL071 Child Syndrome 58 0.113
81
MDY003 Mody, Type Ii 38 0.113
82
KDS001 Kid Syndrome 53 0.113
83
ORL015 Oral Squamous Cell Carcinoma 56 0.113
84
c HPT016 Hepatitis B 64 0.113
85
PRM025 Primary Bacterial Infectious Disease 43 0.112
86
P MYL006 Myeloid Leukemia 67 0.112
87
STM007 Stomatitis 50 0.111
88
PHR003 Pharyngitis 58 0.111
89
VRL011 Viral Infectious Disease 59 0.110
90
P OVR042 Ovarian Cancer 75 0.110
91
GST050 Gastrointestinal System Disease 54 0.110
92
TNG009 Tongue Squamous Cell Carcinoma 74 0.109
93
SPL039 Split Foot 33 0.108
94
HDN004 Head and Neck Carcinoma 55 0.107
95
ALN001 Aland Island Eye Disease 45 0.107
96
c SYS001 Systemic Lupus Erythematosus 87 0.107
97
CSY001 C Syndrome 49 0.106
98
ATM052 Autoimmune Disease 1 28 0.105
99
ATM053 Autoimmune Disease 2 19 0.105
100
HRP001 Herpangina 27 0.105
101
BLD054 Blood Protein Disease 40 0.105
102
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.105
103
NSD001 Nose Disease 52 0.104
104
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.104
105
URN009 Urinary System Disease 53 0.103
106
P URF003 Urofacial Syndrome 1 52 0.103
107
SKN027 Skin Conditions 45 0.103
108
CTS003 Coats Disease 57 0.103
109
ALR002 Al-Raqad Syndrome 36 0.102
110
C3D001 C3 Deficiency 53 0.102
111
IMM136 Immune System Disease 50 0.102
112
WLL006 Wells Syndrome 56 0.101
113
P HMR003 Hemorrhagic Disease 57 0.100
114
P CLL015 Collagen Disease 49 0.100
115
GDS001 Good Syndrome 45 0.100
116
P MNN013 Meningitis 65 0.100
117
P EXN002 Exanthem 57 0.100
118
P PSR002 Psoriasis 63 0.100
119
CRV038 Cervical Squamous Cell Carcinoma 59 0.099
120
BCK006 Back Pain 42 0.099
121
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.099
122
VSC008 Vascular Hemostatic Disease 33 0.099
123
MRG013 Mirage Syndrome 26 0.098
124
P GST049 Gastrointestinal System Cancer 60 0.098
125
GLB003 Globe Disease 35 0.097
126
VSC006 Vascular Cancer 54 0.096
127
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.096
128
SXL003 Sexual Disorder 47 0.096
129
P LYM026 Lymphoblastic Leukemia 60 0.096
130
P HYP086 Hypothyroidism 65 0.096
131
c AST039 Asthma 2 31 0.096
132
AYM001 Ayme-Gripp Syndrome 45 0.096
133
P BCL006 B-Cell Lymphomas 64 0.096
134
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.095
135
CRD118 Cardiovascular Cancer 47 0.095
136
ADJ001 Adjustment Disorder 38 0.094
137
DSS008 Disease of Mental Health 55 0.094
138
MDD011 Mood Disorder 61 0.094
139
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.094
140
c HYP595 Hypertension, Essential 69 0.094
141
c AST037 Asthma 1 31 0.093
142
KWS002 Kawasaki Disease 70 0.092
143
LYM024 Lymphatic System Disease 50 0.092
144
P LYM033 Lymphoproliferative Syndrome 53 0.091
145
c CRN175 Coronary Heart Disease 4 21 0.091
146
EXF001 Exfoliation Syndrome 57 0.091
147
ANX002 Anxiety Disorder 69 0.091
148
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.091
149
HMT002 Hematologic Cancer 64 0.090
150
VRR004 Verrucous Carcinoma 53 0.090
151
ATM054 Autoimmune Disease 3 18 0.090
152
STM006 Stomach Disease 50 0.090
153
c CLL013 Cell Type Cancer 48 0.090
154
SPN369 Spinal Disease 41 0.089
155
c ACT073 Acute Leukemia 62 0.089
156
P BLD051 Blood Coagulation Disease 45 0.089
157
BNC003 Bone Cancer 45 0.089
158
P PLN008 Peeling Skin Syndrome 47 0.089
159
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.089
160
P NSP012 Nasopharyngeal Carcinoma 67 0.088
161
P MSC005 Muscular Dystrophy 64 0.088
162
c CRN214 Coronary Heart Disease 5 23 0.087
163
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.087
164
ATM005 Autoimmune Disease of Musculoskeletal System 16 0.086
165
ORL014 Oral Pharyngeal Disorders 14 0.086
166
BNF002 Bone Fracture 47 0.085
167
LYM019 Lymphosarcoma 53 0.085
168
ORP003 Oropharynx Cancer 47 0.085
169
ATM055 Autoimmune Disease 4 18 0.085
170
P LPC002 Lip Cancer 53 0.084
171
VSC011 Vasculitis 62 0.084
172
P RHN004 Rhinitis 61 0.084
173
P CRN178 Coronary Heart Disease 6 24 0.083
174
P DYS154 Dystonia 64 0.083
175
HDC001 Headache 54 0.083
176
PRD011 Proud Syndrome 42 0.083
177
HDN002 Head Injury 45 0.083
178
VSC047 Vascular Malformation 45 0.082
179
P ACT135 Acute Graft Versus Host Disease 53 0.082
180
HDG012 Hodgkin Lymphoma 73 0.082
181
PMP001 Pemphigus 49 0.082
182
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.081
183
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.081
184
BNM001 Bone Marrow Cancer 52 0.081
185
ATM059 Autoimmune Disease 6 26 0.081
186
P END044 Endometriosis 53 0.080
187
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 36 0.079
188
P OVR049 Ovarian Disease 55 0.079
189
c INF067 Inflammatory Bowel Disease 10 51 0.079
190
MSL001 Measles 61 0.079
191
SNS023 Sensory System Cancer 46 0.078
192
RDT005 Radiation Induced Cancer 28 0.078
193
RPR002 Reproductive System Disease 46 0.078
194
OPT006 Optic Nerve Disease 51 0.078
195
ATN003 Autonomic Nervous System Neoplasm 43 0.078
196
BLD044 Bladder Disease 51 0.077
197
RDN001 Reading Disorder 39 0.077
198
ANG049 Angioedema Induced by Ace Inhibitors 35 0.077
199
P RSP003 Respiratory Failure 70 0.077
200
c PRM023 Pre-Malignant Neoplasm 43 0.076
201
P SLP006 Sleep Apnea 61 0.076
202
c CHR579 Chiari Malformation Type Ii 38 0.076
203
FST001 Foster-Kennedy Syndrome 34 0.076
204
LKC003 Leukocyte Disease 47 0.075
205
P MYS005 Myositis 56 0.075
206
DWN001 Down Syndrome 65 0.075
207
DFF005 Diffuse Large B-Cell Lymphoma 56 0.074
208
TTN003 Tetanus 61 0.074
209
SFT003 Soft Tissue Sarcoma 56 0.074
210
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.073
211
CRB025 Carbohydrate Metabolic Disorder 47 0.073
212
LYM115 Lymphoma, Non-Hodgkin 65 0.073
213
DMY004 Demyelinating Disease 55 0.072
214
FML038 Female Reproductive Organ Cancer 51 0.072
215
c PLN017 Peeling Skin Syndrome 1 33 0.072
216
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.072
217
P LRY044 Larynx Cancer 59 0.072
218
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.072
219
OBS061 Obstructive Sleep Apnea 66 0.071
220
VGN023 Vaginitis 42 0.071
221
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.071
222
TNG004 Tongue Disease 41 0.071
223
LPD004 Lipoid Nephrosis 48 0.071
224
LYM067 Lymphoid Leukemia 43 0.070
225
ATR060 Atrial Standstill, Digenic 53 0.070
226
P LTR001 Lateral Sclerosis 52 0.070
227
PPL022 Papilloma 55 0.070
228
P ACT074 Acute Lymphocytic Leukemia 55 0.070
229
c INF071 Inflammatory Bowel Disease 1 51 0.070
230
c BSL007 Basal Cell Carcinoma 64 0.069
231
SPN051 Spondylitis 50 0.069
232
ECT006 Ectodermal Dysplasia 47 0.069
233
P RTT002 Rett Syndrome 78 0.068
234
P MYL005 Myelofibrosis 67 0.068
235
SPC010 Speech and Communication Disorders 46 0.068
236
P MSC003 Muscular Atrophy 51 0.068
237
WST001 West Syndrome 61 0.068
238
P CNJ013 Conjunctivitis 65 0.068
239
SXD001 Sex Differentiation Disease 40 0.067
240
P OST028 Osteochondroma 48 0.067
241
THY028 Thyroid Cancer 68 0.067
242
SPN041 Spinal Cord Disease 48 0.067
243
BLL006 Bullous Pemphigoid 58 0.067
244
HNS001 Hansen's Disease 29 0.066
245
RST001 Restless Legs Syndrome 54 0.066
246
ADR038 Adermatoglyphia 48 0.066
247
ATN005 Autonomic Dysfunction 45 0.066
248
P CNN004 Connective Tissue Cancer 45 0.066
249
P END033 Endocarditis 52 0.066
250
SPC003 Specific Developmental Disorder 40 0.065
251
CRY003 Cryptosporidiosis 46 0.065
252
CLL003 Cellulitis 49 0.065
253
LYM040 Lymphoblastic Lymphoma 54 0.065
254
c PLN021 Peeling Skin Syndrome 3 31 0.065
255
P LPS002 Liposarcoma 50 0.064
256
c PLN018 Peeling Skin Syndrome 2 35 0.064
257
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.064
258
CNT047 Contact Dermatitis 62 0.064
259
LSH001 Leishmaniasis 62 0.063
260
ACR007 Acromegaly 65 0.063
261
NSL022 Nasal Cavity Disease 42 0.063
262
MNT001 Mantle Cell Lymphoma 70 0.063
263
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.062
264
LYM027 Lymphopenia 54 0.062
265
BRC012 Brucellosis 65 0.062
266
P PRD006 Prader-Willi Syndrome 63 0.062
267
c LKM062 Leukemia, Acute Lymphoblastic 64 0.062
268
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.061
269
NRF007 Neurofibroma 52 0.061
270
P TRT010 Teratoma 52 0.061
271
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.061
272
P TRC086 Trichohepatoenteric Syndrome 1 46 0.060
273
SNS003 Sensory Peripheral Neuropathy 47 0.060
274
P FML035 Familial Hyperlipidemia 50 0.060
275
c ADL052 Adult Acute Lymphocytic Leukemia 42 0.060
276
P MYT002 Myotonic Dystrophy 47 0.060
277
PLG002 Plague 49 0.059
278
LPM004 Lipoma 58 0.059
279
TNG003 Tongue Cancer 60 0.059
280
PST028 Post-Traumatic Stress Disorder 57 0.059
281
RHB003 Rhabdomyosarcoma 58 0.059
282
CYT008 Cytomegalovirus Infection 51 0.059
283
FDL002 Food Allergy 54 0.059
284
P SHR029 Short Syndrome 60 0.058
285
FXF002 Fox-Fordyce Disease 39 0.058
286
ANK001 Ankylosis 52 0.058
287
ADT003 Auditory System Disease 51 0.058
288
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.058
289
P MLT074 Multiple Endocrine Neoplasia 55 0.058
290
WLL001 Williams-Beuren Syndrome 61 0.058
291
MLN007 Male Infertility 56 0.058
292
PLM010 Pulmonary Edema 56 0.057
293
c CHR096 Chronic Pulmonary Heart Disease 40 0.057
294
c ADL017 Adult T-Cell Leukemia 58 0.057
295
MXD023 Mixed Cell Type Cancer 47 0.056
296
c SPL024 Split-Hand/foot Malformation 3 27 0.056
297
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.056
298
PGT001 Paget's Disease of Bone 59 0.056
299
SVR004 Severe Combined Immunodeficiency 68 0.056
300
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.056
301
P ANG015 Angioedema 53 0.056
302
P SPN046 Spinal Muscular Atrophy 63 0.055
303
c OST147 Osteoarthritis 1 33 0.055
304
c CNN010 Connective Tissue Benign Neoplasm 35 0.055
305
YLL002 Yellow Fever 57 0.055
306
NSY001 N Syndrome 39 0.055
307
SPL012 Splenic Disease 47 0.055
308
BBS001 Babesiosis 45 0.054
309
CRY004 Cryoglobulinemia 47 0.054
310
P AML002 Amelogenesis Imperfecta 43 0.054
311
HPT074 Hepatic Adenoma, Somatic 51 0.053
312
GNC005 Geniculate Ganglionitis 31 0.053
313
FCL011 Facial Nerve Disease 38 0.053
314
SMT004 Smith-Lemli-Opitz Syndrome 67 0.053
315
SCR011 Scrapie 39 0.053
316
SYS003 Systolic Heart Failure 43 0.053
317
AND005 Androgen Insensitivity Syndrome, Mild 16 0.052
318
SCR015 Scarlet Fever 39 0.052
319
MST005 Mastitis 52 0.052
320
NRL005 Neurilemmoma 51 0.052
321
P ANG001 Angelman Syndrome 61 0.052
322
MLG097 Malignant Mesenchymal Tumor 37 0.051
323
ANX004 Anoxia 44 0.051
324
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.051
325
c MLT136 Multiple Endocrine Neoplasia 1 68 0.051
326
CRV045 Cervical Intraepithelial Neoplasia 38 0.051
327
FCT008 Factitious Disorder 43 0.051
328
SPC005 Speech Disorder 43 0.051
329
P LKD001 Leukodystrophy 58 0.051
330
c ATM093 Autoimmune Disease of Peripheral Nervous System 35 0.051
331
SWN001 Swine Influenza 37 0.051
332
ABL002 Ablepharon-Macrostomia Syndrome 57 0.050
333
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.050
334
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.050
335
MYC033 Myoclonus 41 0.050
336
KPS004 Kaposi Sarcoma 66 0.049
337
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.049
338
P NLD001 Nail Disease 56 0.049
339
TCK001 Tick-Borne Encephalitis 49 0.049
340
ORL012 Oral Leukoplakia 46 0.049
341
CHN016 Cohen Syndrome 55 0.048
342
WLF002 Wolf-Hirschhorn Syndrome 45 0.048
343
HYP016 Hypochondriasis 39 0.048
344
TRG002 Trigeminal Neuralgia 56 0.048
345
ACR014 Acral Lentiginous Melanoma 44 0.048
346
CHC001 Chickenpox 52 0.048
347
CLF004 Cleft Lip/palate 46 0.048
348
OVR094 Ovarian Epithelial Cancer 45 0.048
349
SYN036 Syncope 47 0.048
350
c VRL007 Viral Encephalitis 54 0.047
351
P SYS005 Systemic Scleroderma 58 0.047
352
TWN003 Townes-Brocks Syndrome 53 0.047
353
c INS002 in Situ Carcinoma 52 0.047
354
ASP003 Aseptic Meningitis 51 0.047
355
P GNR027 Generalized Peeling Skin Syndrome 22 0.047
356
GGN002 Gigantism 27 0.046
357
ATR076 Atrophic Muscular Disease 18 0.046
358
PTZ001 Peutz-Jeghers Syndrome 70 0.046
359
PTR006 Peters Anomaly 64 0.046
360
PRT035 Peritoneum Cancer 39 0.045
361
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.045
362
P ART121 Arthrogryposis Multiplex Congenita, Distal, Type 1 42 0.045
363
DNG002 Dengue Hemorrhagic Fever 62 0.045
364
TTR016 Tetra-Amelia Syndrome 36 0.045
365
c ART117 Arthrogryposis, Distal, Type 2b 37 0.044
366
P LFR001 Li-Fraumeni Syndrome 75 0.044
367
P PHR004 Pharynx Cancer 42 0.044
368
P SLP003 Salpingitis 32 0.044
369
NCR007 Necrotizing Fasciitis 45 0.044
370
P SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 48 0.044
371
DNG003 Dengue Disease 58 0.044
372
P GRN010 Granular Cell Tumor 47 0.044
373
P ART061 Arthrogryposis, Distal, Type 2a 52 0.044
374
P CTN003 Cutaneous Lupus Erythematosus 50 0.044
375
OST011 Osteomalacia 48 0.044
376
c INF023 Inflammatory Breast Carcinoma 50 0.044
377
CYS014 Cystadenocarcinoma 46 0.043
378
URB001 Urbach-Wiethe Disease 48 0.043
379
c SPN225 Spondyloarthropathy 1 63 0.043
380
VNZ002 Venezuelan Equine Encephalitis 44 0.043
381
PTY004 Pityriasis Lichenoides 24 0.043
382
P TRC072 Treacher Collins Syndrome 1 52 0.042
383
P RBN001 Rubinstein-Taybi Syndrome 65 0.042
384
P PTT014 Pitt-Hopkins Syndrome 51 0.042
385
P SLV001 Silver-Russell Syndrome 54 0.042
386
PHT003 Phototoxic Dermatitis 38 0.042
387
P VLC001 Velocardiofacial Syndrome 62 0.042
388
LYM127 Lymphatic Malformations 37 0.042
389
P DSB006 Desbuquois Dysplasia 1 53 0.042
390
FLL029 Fallopian Tube Disease 34 0.042
391
c NPH055 Nephrotic Syndrome, Type 1 59 0.042
392
P CWD006 Cowden Syndrome 1 68 0.042
393
PYG006 Pyogenic Granuloma 41 0.042
394
P ESC003 Escobar Syndrome 58 0.042
395
P CRN139 Cornelia De Lange Syndrome 1 60 0.041
396
HNM002 Hinman Syndrome 25 0.041
397
OCL011 Ocular Motility Disease 38 0.041
398
RTR008 Root Resorption 41 0.041
399
ANG037 Angiomatosis 34 0.040
400
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.040
401
PLX002 Plexiform Neurofibroma 42 0.040
402
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.040
403
AMB001 Amebiasis 42 0.040
404
INV006 Inverted Papilloma 40 0.040
405
FBR011 Fibrodysplasia Ossificans Progressiva 62 0.040
406
RNP001 Renpenning Syndrome 48 0.040
407
CRB150 Cerebral Creatine Deficiency Syndrome 2 48 0.039
408
HYP622 Hypertrichotic Osteochondrodysplasia 38 0.039
409
HNT002 Hantavirus Pulmonary Syndrome 51 0.039
410
FRY002 Fryns Syndrome 36 0.039
411
P DNT011 Dentinogenesis Imperfecta 42 0.039
412
BWN001 Bowen-Conradi Syndrome 45 0.039
413
PTY006 Pityriasis Lichenoides Et Varioliformis Acuta 20 0.039
414
P WVR001 Weaver Syndrome 51 0.039
415
P EMB005 Embryonal Rhabdomyosarcoma 54 0.039
416
ARS001 Aarskog-Scott Syndrome 52 0.039
417
P HLL001 Hallermann-Streiff Syndrome 53 0.039
418
LRN006 Laurin-Sandrow Syndrome 31 0.039
419
CHR222 Chromosome 1p36 Deletion Syndrome 41 0.039
420
MYB001 Myoblastoma 22 0.039
421
c RBN009 Robinow Syndrome, Autosomal Recessive 32 0.038
422
ACR043 Acromicric Dysplasia 30 0.038
423
INT104 Intravascular Papillary Endothelial Hyperplasia 31 0.038
424
c INF093 Inflammatory Bowel Disease 14 23 0.038
425
LDD001 Ladd Syndrome 60 0.038
426
ACR008 Acrocallosal Syndrome 51 0.038
427
PST010 Pasteurellosis 34 0.038
428
c JBR020 Joubert Syndrome 1 59 0.038
429
P MWT001 Mowat-Wilson Syndrome 46 0.038
430
DST005 Diastrophic Dysplasia 52 0.038
431
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 56 0.038
432
c OTP007 Otopalatodigital Syndrome, Type Ii 37 0.037
433
PLM017 Pulmonary Alveolar Microlithiasis 46 0.037
434
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 32 0.037
435
PMP008 Pemphigus Vegetans 24 0.037
436
CHR101 Char Syndrome 29 0.037
437
ADP007 Adie Pupil 34 0.037
438
P CYS017 Cystic Teratoma 41 0.037
439
BRN105 Burn Scar 37 0.037
440
ARM006 Armfield X-Linked Mental Retardation Syndrome 18 0.036
441
DBW001 Dubowitz Syndrome 46 0.036
442
BSL006 Basaloid Squamous Cell Carcinoma 41 0.036
443
P LRS001 Larsen Syndrome 51 0.036
444
c ICH041 Ichthyosis, Autosomal Recessive 4b 35 0.036
445
MBS002 Moebius Syndrome 44 0.036
446
FNT004 Fainting 33 0.036
447
c CMP072 Camptodactyly Syndrome, Guadalajara, Type I 17 0.036
448
GLS018 Glass Syndrome 35 0.035
449
SPN006 Spindle Cell Lipoma 34 0.035
450
P RST011 Restrictive Dermopathy, Lethal 38 0.035
451
INN003 Iniencephaly 24 0.035
452
SCT005 Scott Syndrome 50 0.035
453
MNT231 Mental Retardation, X-Linked Syndromic, Nascimento-Type 25 0.035
454
PDT040 Pediatric Hypertension 31 0.035
455
SCR033 Scar Contracture 26 0.035
456
CNT001 Contagious Pustular Dermatitis 34 0.035
457
P MNN007 Meningocele 36 0.035
458
RHN003 Rhinosporidiosis 33 0.035
459
ACR013 Acrodysostosis 49 0.034
460
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 45 0.034
461
P MCK022 Meckel Syndrome 1 53 0.034
462
FCD002 Faciodigitogenital Syndrome, Autosomal Recessive 14 0.034
463
SMT006 Somatoform Disorder 53 0.034
464
c ATL002 Atelosteogenesis Ii 26 0.034
465
LTH002 Lathosterolosis 29 0.034
466
P NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 57 0.034
467
SMT001 Somatization Disorder 46 0.034
468
ACR058 Acrofacial Dysostosis 1, Nager Type 36 0.033
469
CHR382 Chromosome 18q Deletion Syndrome 32 0.033
470
RNS001 Raine Syndrome 39 0.033
471
CHR399 Chromosome 4q21 Deletion Syndrome 22 0.033
472
ACH032 Achondrogenesis, Type Ii or Hypochondrogenesis 51 0.033
473
PLL008 Pallister-Killian Syndrome 31 0.033
474
MHR002 Mohr Syndrome 28 0.032
475
P CRD013 Cardiofaciocutaneous Syndrome 63 0.032
476
BRC097 Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation 21 0.032
477
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.032
478
2Q3005 2q31.1 Microdeletion Syndrome 16 0.032
479
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 32 0.032
480
MTR010 Mature Teratoma 42 0.032
481
CHR543 Chromosome 2q37 Deletion Syndrome 29 0.032
482
LPR018 Leprechaunism 59 0.032
483
P FRN012 Frontometaphyseal Dysplasia 38 0.032
484
ADN020 Adenosarcoma 38 0.031
485
c ORF037 Orofaciodigital Syndrome I 46 0.031
486
OHD004 Ohdo Syndrome 32 0.031
487
PLY056 Polyposis, Juvenile Intestinal 55 0.031
488
RVL002 Ruvalcaba Syndrome 31 0.031
489
CHR386 Chromosome 6pter-P24 Deletion Syndrome 35 0.031
490
FNT003 Fountain Syndrome 27 0.031
491
c MNT109 Mental Retardation, X-Linked, Syndromic 15 31 0.030
492
CDL003 Caudal Regression Syndrome 51 0.030
493
SPN113 Spinocerebellar Ataxia with Dysmorphism 18 0.030
494
ECZ002 Eczema Herpeticum 46 0.030
495
PRP082 Porphyria, Congenital Erythropoietic 46 0.030
496
HJD001 Hajdu-Cheney Syndrome 58 0.029
497
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 47 0.029
498
URT016 Urethral Diverticulum 30 0.029
499
ONC003 Oncogenic Osteomalacia 40 0.029
500
CHR105 Choreoacanthocytosis 45 0.029
501
BLR027 Blue Rubber Bleb Nevus 33 0.029
502
P KLN006 Koolen-De Vries Syndrome 37 0.029
503
SNW001 Snowflake Vitreoretinal Degeneration 39 0.029
504
TRN066 Transmitted_by 24 0.029
505
NCR003 Necrotizing Sialometaplasia 34 0.028
506
P DNT009 Dentin Dysplasia 37 0.028
507
PRG123 Progeroid Syndrome, Neonatal 23 0.028
508
CHN050 Chondrodysplasia with Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, and Microphthalmia 21 0.028
509
P CNG046 Congenital Fiber-Type Disproportion 48 0.028
510
THY049 Thyroid Cancer, Anaplastic 41 0.028
511
SPR038 Supranuclear Ocular Palsy 20 0.027
512
c GLP003 Geleophysic Dysplasia 1 26 0.027
513
c LRS002 Larsen-Like Syndrome 36 0.027
514
P FTL009 Fetal Akinesia Deformation Sequence 49 0.027
515
PPL003 Papillary Cystadenocarcinoma 37 0.027
516
TNS004 Tonsil Cancer 44 0.027
517
MSM004 Mesomelia-Synostoses Syndrome 23 0.027
518
PSD046 Pseudotrisomy 13 Syndrome 23 0.027
519
c CRN134 Cornelia De Lange Syndrome 2 26 0.027
520
SCH071 Schaaf-Yang Syndrome 26 0.027
521
CHR224 Chromosome 1q Duplication 19 0.026
522
CHR229 Chromosome 20p Duplication 18 0.026
523
MCR308 Microcephalic Primordial Dwarfism, Toriello Type 17 0.026
524
P OTP001 Otopalatodigital Syndrome 25 0.026
525
CHM006 Chime Syndrome 33 0.026
526
20P001 20p12.3 Microdeletion Syndrome 12 0.026
527
8Q1001 8q12 Microduplication Syndrome 11 0.026
528
c ORF035 Orofaciodigital Syndrome Iv 26 0.026
529
MCR063 Microcephaly, Holoprosencephaly, and Intrauterine Growth Retardation 6 0.026
530
c CRN209 Cornelia De Lange Syndrome 5 24 0.025
531
c FBR029 Fibrochondrogenesis 1 19 0.025
532
MNT121 Mental Retardation, X-Linked Syndromic, Christianson Type 30 0.025
533
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 21 0.025
534
MMS001 Momo Syndrome 22 0.025
535
WLS004 Wilson-Turner Syndrome 30 0.024
536
GRC002 Gracile Bone Dysplasia 27 0.024
537
SPN141 Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech 14 0.024
538
c EHL025 Ehlers-Danlos Syndrome, Musculocontractural Type 30 0.024
539
CHN043 Chondrodysplasia with Joint Dislocations, Grapp Type 20 0.023
540
CHR212 Chromosome 18p Duplication 16 0.022
541
DPL009 Duplication of the Pituitary Gland 17 0.022
542
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 12 0.022
543
8PN001 8p Inverted Duplication/deletion Syndrome 12 0.021
544
XLN135 X-Linked Intellectual Disability, Vitale Type 8 0.021
545
SCH031 Scholte Syndrome 11 0.021