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"

547 hits were found for 'foot and mouth disease'

# Family MCID Name MIFTS Score
1
HND002 Hand, Foot and Mouth Disease 49 4.046
2
MTH009 Mouth Disease 63 0.644
3
BRN106 Burns 52 0.287
4
P NRP001 Neuropathy 57 0.283
5
P ART022 Arthritis 73 0.224
6
END072 Endotheliitis 41 0.219
7
P HPT021 Hepatitis 74 0.216
8
P LKM002 Leukemia 70 0.207
9
c MCR129 Microvascular Complications of Diabetes 1 55 0.203
10
CRB009 Cerebritis 36 0.198
11
P LYM118 Lymphoma 68 0.197
12
FTD001 Foot Drop 34 0.196
13
PRP027 Peripheral Vascular Disease 69 0.177
14
P RHM011 Rheumatoid Arthritis 87 0.175
15
VSC007 Vascular Disease 51 0.172
16
SKN016 Skin Disease 69 0.171
17
ORL011 Oral Cancer 53 0.167
18
P ORL007 Oral Cavity Cancer 58 0.166
19
P ART023 Arthropathy 63 0.162
20
MLN008 Melanoma 61 0.160
21
P CLR023 Colorectal Cancer 96 0.158
22
c PND001 Pain Disorder 53 0.158
23
P AST005 Asthma 80 0.156
24
SRC014 Sarcoma 66 0.155
25
P PRD008 Periodontitis 46 0.154
26
TTH006 Tooth Disease 52 0.151
27
SKN027 Skin Conditions 44 0.147
28
ADM013 Adamantinoma of Long Bones 57 0.145
29
P NRV007 Nervous System Disease 71 0.145
30
c CNT035 Central Nervous System Disease 60 0.143
31
P MYP004 Myopathy 67 0.141
32
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.141
33
P ENC004 Encephalitis 60 0.141
34
NTR005 Nutritional Deficiency Disease 51 0.141
35
DRM006 Dermatitis 58 0.140
36
ATH003 Atherosclerosis 63 0.140
37
RSP006 Respiratory System Disease 61 0.140
38
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.139
39
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.138
40
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.138
41
NRM005 Neuromuscular Disease 56 0.137
42
SPL040 Split Hand 35 0.136
43
PRP019 Peripheral Nervous System Disease 52 0.135
44
ADL002 Adult Syndrome 53 0.134
45
TBR010 Tuberculosis 70 0.134
46
P CRV039 Cervicitis 45 0.133
47
BRT030 Birth Defects 44 0.133
48
RHM027 Rheumatic Disease 55 0.132
49
MVM001 Movement Disease 45 0.132
50
JNT002 Joint Disorders 55 0.131
51
P INF038 Influenza 71 0.130
52
P SPS003 Spastic Diplegia 49 0.129
53
P PNM007 Pneumonia 67 0.129
54
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.129
55
CNN005 Connective Tissue Disease 60 0.128
56
PCK002 Pick Disease 66 0.128
57
P NRV006 Nervous System Cancer 62 0.127
58
APH001 Aphthous Stomatitis 62 0.125
59
HYP266 Hypoxia 55 0.125
60
ACR041 Acromelic Frontonasal Dysostosis 45 0.124
61
ALR002 Al-Raqad Syndrome 36 0.123
62
CRH001 Crohn's Disease 76 0.122
63
P INF032 Infertility 61 0.120
64
P CHR345 Chronic Pain 45 0.120
65
P MSC033 Muscle Disorders 52 0.120
66
ATN002 Autonomic Nervous System Disease 46 0.120
67
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.119
68
PHY002 Physical Disorder 43 0.118
69
P SCH015 Schizophrenia 78 0.118
70
BNS002 Bone Structure Disease 37 0.117
71
P CLL015 Collagen Disease 49 0.117
72
ANR040 Aneurysm 56 0.117
73
SLP005 Sleep Disorder 52 0.117
74
OCL009 Ocular Cancer 61 0.117
75
P LPS004 Lupus Erythematosus 63 0.116
76
ORL015 Oral Squamous Cell Carcinoma 55 0.116
77
PRP021 Peripheral Nervous System Neoplasm 49 0.116
78
GST050 Gastrointestinal System Disease 58 0.116
79
VND001 Vein Disease 51 0.116
80
MSC004 Muscle Tissue Disease 35 0.116
81
STM007 Stomatitis 50 0.115
82
c HPT016 Hepatitis B 61 0.115
83
SPN041 Spinal Cord Disease 50 0.115
84
SPL039 Split Foot 32 0.115
85
P MYL006 Myeloid Leukemia 67 0.114
86
MDY003 Mody, Type Ii 36 0.114
87
ALN001 Aland Island Eye Disease 45 0.114
88
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.114
89
GST053 Gastric Cancer 52 0.114
90
VRL011 Viral Infectious Disease 56 0.114
91
BRS051 Breast Disease 57 0.114
92
TNG009 Tongue Squamous Cell Carcinoma 73 0.113
93
C3D001 C3 Deficiency 50 0.112
94
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.112
95
KDS001 Kid Syndrome 53 0.111
96
PHR003 Pharyngitis 58 0.111
97
CHL071 Child Syndrome 58 0.111
98
ALL026 Allergic Hypersensitivity Disease 53 0.111
99
HDN004 Head and Neck Carcinoma 54 0.110
100
PRM025 Primary Bacterial Infectious Disease 42 0.110
101
EYD002 Eye Disease 62 0.110
102
BLD054 Blood Protein Disease 38 0.110
103
PRD007 Periodontal Disease 42 0.109
104
P OVR042 Ovarian Cancer 73 0.109
105
LRN003 Learning Disability 49 0.109
106
P LFR001 Li-Fraumeni Syndrome 79 0.108
107
c SYS001 Systemic Lupus Erythematosus 87 0.107
108
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.106
109
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.106
110
ATM052 Autoimmune Disease 1 26 0.106
111
CSY001 C Syndrome 49 0.106
112
HRP001 Herpangina 26 0.105
113
ATM053 Autoimmune Disease 2 16 0.105
114
P MNN013 Meningitis 66 0.104
115
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.104
116
NSD001 Nose Disease 51 0.103
117
CRV038 Cervical Squamous Cell Carcinoma 58 0.103
118
P EXN002 Exanthem 57 0.103
119
ACQ007 Acquired Immunodeficiency Syndrome 60 0.102
120
CTS003 Coats Disease 57 0.102
121
INC022 Inclusion-Cell Disease 46 0.102
122
GLB003 Globe Disease 34 0.102
123
P GST049 Gastrointestinal System Cancer 59 0.101
124
P HYP086 Hypothyroidism 63 0.101
125
WLL006 Wells Syndrome 57 0.100
126
P PSR002 Psoriasis 63 0.100
127
c CLL013 Cell Type Cancer 46 0.100
128
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.100
129
GDS001 Good Syndrome 46 0.100
130
URN009 Urinary System Disease 52 0.100
131
VSC006 Vascular Cancer 51 0.100
132
SXL003 Sexual Disorder 45 0.099
133
BCK006 Back Pain 40 0.099
134
KWS002 Kawasaki Disease 70 0.099
135
P BCL006 B-Cell Lymphomas 64 0.098
136
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.098
137
VSC008 Vascular Hemostatic Disease 30 0.098
138
MDD011 Mood Disorder 60 0.098
139
AYM001 Ayme-Gripp Syndrome 40 0.097
140
P LYM026 Lymphoblastic Leukemia 60 0.096
141
ANX002 Anxiety Disorder 67 0.096
142
c AST039 Asthma 2 28 0.095
143
ETH011 Ethylmalonic Encephalopathy 57 0.095
144
HMT002 Hematologic Cancer 62 0.095
145
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.094
146
ADJ001 Adjustment Disorder 38 0.093
147
c AST037 Asthma 1 35 0.092
148
MVD001 Moved to 60 0.092
149
VRR004 Verrucous Carcinoma 54 0.091
150
LYM024 Lymphatic System Disease 49 0.091
151
VSC011 Vasculitis 62 0.091
152
P MSC005 Muscular Dystrophy 64 0.091
153
LYM023 Lymphatic System Cancer 35 0.091
154
BRN071 Brain Injury 51 0.090
155
ATM054 Autoimmune Disease 3 16 0.090
156
BNC003 Bone Cancer 44 0.090
157
STM006 Stomach Disease 48 0.089
158
P NSP012 Nasopharyngeal Carcinoma 59 0.089
159
c ACT073 Acute Leukemia 61 0.089
160
RPR002 Reproductive System Disease 45 0.089
161
P BLD051 Blood Coagulation Disease 44 0.089
162
ORP003 Oropharynx Cancer 48 0.089
163
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.088
164
P LPC002 Lip Cancer 50 0.088
165
FML039 Female Reproductive System Disease 49 0.088
166
P RHN004 Rhinitis 59 0.086
167
EXF001 Exfoliation Syndrome 56 0.086
168
LYM019 Lymphosarcoma 52 0.086
169
c CRN214 Coronary Heart Disease 5 22 0.086
170
MSL001 Measles 61 0.086
171
ORL014 Oral Pharyngeal Disorders 13 0.086
172
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.086
173
ATM005 Autoimmune Disease of Musculoskeletal System 14 0.086
174
BNF002 Bone Fracture 46 0.085
175
HDG012 Hodgkin Lymphoma 75 0.085
176
P LRY016 Laryngeal Carcinoma 60 0.084
177
ATM055 Autoimmune Disease 4 16 0.084
178
PMP001 Pemphigus 49 0.084
179
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.084
180
P CRN178 Coronary Heart Disease 6 22 0.084
181
P PLN008 Peeling Skin Syndrome 45 0.083
182
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.083
183
HDC001 Headache 52 0.083
184
P END044 Endometriosis 53 0.082
185
PRD011 Proud Syndrome 42 0.082
186
P NPH012 Nephrotic Syndrome 55 0.082
187
HPT074 Hepatic Adenoma, Somatic 35 0.082
188
BNM001 Bone Marrow Cancer 56 0.081
189
VSC047 Vascular Malformation 45 0.081
190
c INF067 Inflammatory Bowel Disease 10 31 0.081
191
ATM059 Autoimmune Disease 6 23 0.080
192
END040 Endogenous Depression 51 0.080
193
c PRM023 Pre-Malignant Neoplasm 42 0.080
194
P DYS154 Dystonia 62 0.079
195
P OVR049 Ovarian Disease 54 0.079
196
MNT002 Mental Depression 52 0.079
197
TTN003 Tetanus 62 0.078
198
HDN002 Head Injury 47 0.078
199
SNS023 Sensory System Cancer 45 0.078
200
BLL006 Bullous Pemphigoid 59 0.078
201
LPD004 Lipoid Nephrosis 49 0.078
202
OPT006 Optic Nerve Disease 47 0.078
203
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 34 0.077
204
DFF005 Diffuse Large B-Cell Lymphoma 57 0.077
205
END035 Endocrine Gland Cancer 50 0.077
206
P MYS005 Myositis 57 0.077
207
ATN003 Autonomic Nervous System Neoplasm 43 0.077
208
BLD044 Bladder Disease 50 0.077
209
RDN001 Reading Disorder 39 0.077
210
P SLP006 Sleep Apnea 60 0.076
211
SFT003 Soft Tissue Sarcoma 55 0.076
212
DMY004 Demyelinating Disease 52 0.076
213
LYM115 Lymphoma, Non-Hodgkin 64 0.075
214
ANG049 Angioedema Induced by Ace Inhibitors 35 0.075
215
FML038 Female Reproductive Organ Cancer 50 0.075
216
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.075
217
FST001 Foster-Kennedy Syndrome 31 0.075
218
DWN001 Down Syndrome 65 0.075
219
RDT005 Radiation Induced Cancer 26 0.074
220
CNT047 Contact Dermatitis 62 0.074
221
P LTR001 Lateral Sclerosis 50 0.074
222
VGN023 Vaginitis 41 0.074
223
PPL022 Papilloma 54 0.074
224
c CHR579 Chiari Malformation Type Ii 38 0.074
225
PLM031 Poliomyelitis 59 0.073
226
ECT006 Ectodermal Dysplasia 46 0.073
227
P RSP003 Respiratory Failure 68 0.072
228
CRB025 Carbohydrate Metabolic Disorder 46 0.072
229
ESP021 Esophageal Cancer 75 0.072
230
LKC003 Leukocyte Disease 45 0.072
231
P ACT074 Acute Lymphocytic Leukemia 54 0.072
232
OBS061 Obstructive Sleep Apnea 61 0.072
233
P MSC003 Muscular Atrophy 51 0.071
234
P STM004 Stomach Cancer 73 0.071
235
THY028 Thyroid Cancer 71 0.071
236
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.071
237
LYM067 Lymphoid Leukemia 38 0.070
238
NSP001 Nasopharynx Carcinoma 54 0.070
239
ATR060 Atrial Standstill, Digenic 51 0.070
240
CRY003 Cryptosporidiosis 47 0.070
241
TNG004 Tongue Disease 40 0.069
242
c BSL007 Basal Cell Carcinoma 66 0.069
243
SPN051 Spondylitis 50 0.069
244
c INF071 Inflammatory Bowel Disease 1 51 0.069
245
MNT001 Mantle Cell Lymphoma 72 0.069
246
RST001 Restless Legs Syndrome 51 0.069
247
c PLN017 Peeling Skin Syndrome 1 32 0.068
248
ATN005 Autonomic Dysfunction 44 0.068
249
P MYL005 Myelofibrosis 67 0.068
250
HNS001 Hansen's Disease 30 0.068
251
P RTT002 Rett Syndrome 77 0.068
252
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.067
253
SXD001 Sex Differentiation Disease 39 0.067
254
SPC010 Speech and Communication Disorders 42 0.067
255
P FLL037 Follicular Lymphoma 68 0.067
256
P END033 Endocarditis 52 0.066
257
P OST028 Osteochondroma 45 0.066
258
WST001 West Syndrome 61 0.066
259
PLM010 Pulmonary Edema 56 0.066
260
P CNN004 Connective Tissue Cancer 44 0.066
261
c SPL024 Split-Hand/foot Malformation 3 28 0.065
262
P ANT006 Antiphospholipid Syndrome 60 0.065
263
TRM010 Traumatic Brain Injury 52 0.065
264
CLL003 Cellulitis 49 0.065
265
P LPS002 Liposarcoma 50 0.065
266
LYM027 Lymphopenia 54 0.065
267
LYM040 Lymphoblastic Lymphoma 51 0.065
268
LSH001 Leishmaniasis 63 0.064
269
SPC003 Specific Developmental Disorder 39 0.064
270
P TRC086 Trichohepatoenteric Syndrome 1 46 0.064
271
ACR007 Acromegaly 66 0.064
272
c PLN021 Peeling Skin Syndrome 3 30 0.064
273
NSL022 Nasal Cavity Disease 41 0.064
274
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.064
275
TNG003 Tongue Cancer 59 0.063
276
ADR038 Adermatoglyphia 39 0.063
277
NRF007 Neurofibroma 53 0.063
278
BRC012 Brucellosis 66 0.063
279
P MYT002 Myotonic Dystrophy 46 0.062
280
P PRD006 Prader-Willi Syndrome 64 0.062
281
PST028 Post-Traumatic Stress Disorder 55 0.062
282
PLG002 Plague 49 0.062
283
P TRT010 Teratoma 49 0.062
284
CRY004 Cryoglobulinemia 47 0.062
285
c LKM062 Leukemia, Acute Lymphoblastic 63 0.061
286
SNS003 Sensory Peripheral Neuropathy 44 0.061
287
P FML035 Familial Hyperlipidemia 49 0.060
288
CYT008 Cytomegalovirus Infection 51 0.060
289
c ADL052 Adult Acute Lymphocytic Leukemia 41 0.060
290
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.060
291
MXD023 Mixed Cell Type Cancer 45 0.060
292
SCR015 Scarlet Fever 37 0.060
293
LPM004 Lipoma 59 0.060
294
SVR004 Severe Combined Immunodeficiency 71 0.060
295
FDL002 Food Allergy 56 0.059
296
P SPN046 Spinal Muscular Atrophy 62 0.059
297
RHB003 Rhabdomyosarcoma 55 0.059
298
P SHR029 Short Syndrome 60 0.059
299
ANK001 Ankylosis 52 0.058
300
WLL001 Williams-Beuren Syndrome 61 0.058
301
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.058
302
FXF002 Fox-Fordyce Disease 37 0.058
303
P MLT074 Multiple Endocrine Neoplasia 55 0.058
304
BBS001 Babesiosis 45 0.058
305
P AML002 Amelogenesis Imperfecta 43 0.058
306
MLN007 Male Infertility 56 0.058
307
c CHR096 Chronic Pulmonary Heart Disease 40 0.057
308
c OST147 Osteoarthritis 1 31 0.056
309
PGT001 Paget's Disease of Bone 60 0.056
310
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 31 0.056
311
MST005 Mastitis 53 0.056
312
HYP016 Hypochondriasis 39 0.056
313
SCR011 Scrapie 34 0.056
314
P ANG015 Angioedema 53 0.056
315
ORL012 Oral Leukoplakia 41 0.056
316
CHC001 Chickenpox 50 0.056
317
PLS016 Plasma Cell Leukemia 52 0.055
318
YLL002 Yellow Fever 58 0.055
319
SWN001 Swine Influenza 42 0.055
320
SPL012 Splenic Disease 48 0.055
321
CRV045 Cervical Intraepithelial Neoplasia 41 0.055
322
c CNN010 Connective Tissue Benign Neoplasm 31 0.055
323
NSY001 N Syndrome 42 0.055
324
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.054
325
ACR014 Acral Lentiginous Melanoma 44 0.054
326
P ORG009 Organ System Cancer 45 0.054
327
SYS003 Systolic Heart Failure 42 0.053
328
URB001 Urbach-Wiethe Disease 48 0.052
329
TCK001 Tick-Borne Encephalitis 49 0.052
330
NRL005 Neurilemmoma 47 0.052
331
ASP003 Aseptic Meningitis 51 0.052
332
P LKD001 Leukodystrophy 58 0.052
333
WLF002 Wolf-Hirschhorn Syndrome 50 0.052
334
SMT004 Smith-Lemli-Opitz Syndrome 66 0.052
335
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.051
336
ANX004 Anoxia 45 0.051
337
P PMP005 Pemphigus Vulgaris 47 0.051
338
c INS002 in Situ Carcinoma 51 0.051
339
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.051
340
MLG097 Malignant Mesenchymal Tumor 36 0.051
341
PTY004 Pityriasis Lichenoides 25 0.051
342
FCT008 Factitious Disorder 42 0.050
343
SPC005 Speech Disorder 41 0.050
344
TRG002 Trigeminal Neuralgia 56 0.050
345
ABL002 Ablepharon-Macrostomia Syndrome 51 0.050
346
c MLG079 Malignant Pleural Mesothelioma 54 0.050
347
MYC033 Myoclonus 41 0.050
348
GNC005 Geniculate Ganglionitis 27 0.050
349
FCL011 Facial Nerve Disease 37 0.050
350
KPS004 Kaposi Sarcoma 69 0.050
351
PTZ001 Peutz-Jeghers Syndrome 71 0.049
352
P CTN003 Cutaneous Lupus Erythematosus 49 0.049
353
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.049
354
P NLD001 Nail Disease 56 0.049
355
ACT055 Actinomycosis 42 0.049
356
P PHR004 Pharynx Cancer 45 0.048
357
SYN036 Syncope 45 0.048
358
c SPN225 Spondyloarthropathy 1 62 0.048
359
P SLP003 Salpingitis 32 0.048
360
P SYS005 Systemic Scleroderma 60 0.048
361
TWN003 Townes-Brocks Syndrome 55 0.048
362
PLM017 Pulmonary Alveolar Microlithiasis 46 0.048
363
OVR094 Ovarian Epithelial Cancer 48 0.048
364
PTY006 Pityriasis Lichenoides Et Varioliformis Acuta 22 0.047
365
CHN016 Cohen Syndrome 55 0.047
366
GGN002 Gigantism 29 0.047
367
c MLT136 Multiple Endocrine Neoplasia 1 68 0.047
368
FLL029 Fallopian Tube Disease 33 0.047
369
P TRC072 Treacher Collins Syndrome 1 50 0.047
370
DNG002 Dengue Hemorrhagic Fever 60 0.046
371
LYM127 Lymphatic Malformations 38 0.046
372
P GNR027 Generalized Peeling Skin Syndrome 21 0.046
373
VNZ002 Venezuelan Equine Encephalitis 43 0.046
374
P EMB005 Embryonal Rhabdomyosarcoma 56 0.046
375
BNN003 Bone Inflammation Disease 46 0.046
376
PYG006 Pyogenic Granuloma 47 0.046
377
PTR006 Peters Anomaly 64 0.045
378
P ART121 Arthrogryposis Multiplex Congenita, Distal, Type 1 41 0.045
379
PRT035 Peritoneum Cancer 34 0.045
380
AMB001 Amebiasis 43 0.045
381
RTR008 Root Resorption 41 0.045
382
OST011 Osteomalacia 48 0.044
383
INV006 Inverted Papilloma 43 0.044
384
CYS014 Cystadenocarcinoma 47 0.044
385
ARS001 Aarskog-Scott Syndrome 52 0.044
386
P GRN010 Granular Cell Tumor 46 0.043
387
FCT001 Factor Viii Deficiency 41 0.043
388
P DNT011 Dentinogenesis Imperfecta 42 0.043
389
c INF023 Inflammatory Breast Carcinoma 44 0.043
390
P VLC001 Velocardiofacial Syndrome 64 0.043
391
PLX002 Plexiform Neurofibroma 42 0.043
392
P SLV001 Silver-Russell Syndrome 54 0.043
393
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 56 0.042
394
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 38 0.042
395
P MNN007 Meningocele 37 0.042
396
c ART117 Arthrogryposis, Distal, Type 2b 36 0.042
397
P CRN015 Cornelia De Lange Syndrome 65 0.042
398
FRY002 Fryns Syndrome 37 0.042
399
P ESC003 Escobar Syndrome 59 0.042
400
PHT003 Phototoxic Dermatitis 37 0.042
401
P PTT014 Pitt-Hopkins Syndrome 51 0.042
402
NCR007 Necrotizing Fasciitis 43 0.042
403
DNG003 Dengue Disease 60 0.041
404
PST010 Pasteurellosis 36 0.041
405
P RBN001 Rubinstein-Taybi Syndrome 65 0.041
406
c EHL057 Ehlers-Danlos Syndrome, Type Iv 59 0.041
407
ANG037 Angiomatosis 33 0.041
408
VHW001 Vohwinkel Syndrome 47 0.041
409
P CYS017 Cystic Teratoma 40 0.041
410
BSL006 Basaloid Squamous Cell Carcinoma 40 0.041
411
OCL011 Ocular Motility Disease 41 0.041
412
CHR101 Char Syndrome 35 0.040
413
MTR031 Motor Neuro-Ophthalmic Disorders 22 0.040
414
P HMN013 Hemangiopericytoma 52 0.040
415
LDD001 Ladd Syndrome 60 0.040
416
RNP001 Renpenning Syndrome 48 0.040
417
c DSB006 Desbuquois Dysplasia 1 34 0.039
418
FBR011 Fibrodysplasia Ossificans Progressiva 61 0.039
419
P PCH001 Pachyonychia Congenita 54 0.039
420
P WVR001 Weaver Syndrome 54 0.039
421
LRN006 Laurin-Sandrow Syndrome 32 0.039
422
P HLL001 Hallermann-Streiff Syndrome 53 0.039
423
ACR008 Acrocallosal Syndrome 51 0.039
424
RHN003 Rhinosporidiosis 35 0.039
425
CHR222 Chromosome 1p36 Deletion Syndrome 43 0.039
426
DST005 Diastrophic Dysplasia 57 0.039
427
MYB001 Myoblastoma 23 0.038
428
CRB150 Cerebral Creatine Deficiency Syndrome 2 47 0.038
429
CDL003 Caudal Regression Syndrome 52 0.038
430
NRS001 Neuroschistosomiasis 30 0.038
431
SNW001 Snowflake Vitreoretinal Degeneration 40 0.038
432
HYP622 Hypertrichotic Osteochondrodysplasia 38 0.038
433
VSC012 Vesiculobullous Skin Disease 38 0.038
434
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.038
435
c INF093 Inflammatory Bowel Disease 14 22 0.037
436
P MWT001 Mowat-Wilson Syndrome 50 0.037
437
ACR043 Acromicric Dysplasia 30 0.037
438
TRN066 Transmitted_by 25 0.037
439
PMP008 Pemphigus Vegetans 23 0.037
440
c RBN009 Robinow Syndrome, Autosomal Recessive 31 0.037
441
c OTP007 Otopalatodigital Syndrome, Type Ii 39 0.037
442
c JBR020 Joubert Syndrome 1 57 0.037
443
INT104 Intravascular Papillary Endothelial Hyperplasia 34 0.037
444
DBW001 Dubowitz Syndrome 48 0.037
445
MBS002 Moebius Syndrome 44 0.037
446
P EPD003 Epidermolysis Bullosa Simplex 50 0.036
447
c BNG076 Benign Exophthalmos Syndrome 15 0.036
448
ADN020 Adenosarcoma 37 0.036
449
BRN105 Burn Scar 36 0.036
450
FNT004 Fainting 33 0.036
451
SPN006 Spindle Cell Lipoma 36 0.036
452
SCT005 Scott Syndrome 51 0.036
453
MTR010 Mature Teratoma 41 0.036
454
c CMP072 Camptodactyly Syndrome, Guadalajara, Type I 18 0.036
455
ACR013 Acrodysostosis 50 0.036
456
MGL023 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome, Somatic 34 0.036
457
INN003 Iniencephaly 25 0.035
458
P LRS001 Larsen Syndrome 53 0.035
459
P MCK022 Meckel Syndrome 1 54 0.035
460
P RST011 Restrictive Dermopathy, Lethal 38 0.035
461
c ICH041 Ichthyosis, Autosomal Recessive 4b 35 0.035
462
GLS018 Glass Syndrome 36 0.035
463
P CRD013 Cardiofaciocutaneous Syndrome 65 0.035
464
MTN002 Mite Infestation 30 0.035
465
ARM006 Armfield X-Linked Mental Retardation Syndrome 17 0.035
466
SMT006 Somatoform Disorder 52 0.035
467
CNT001 Contagious Pustular Dermatitis 30 0.035
468
SCR033 Scar Contracture 24 0.035
469
PDT040 Pediatric Hypertension 30 0.034
470
c ART061 Arthrogryposis, Distal, Type 2a 29 0.034
471
FCD002 Faciodigitogenital Syndrome, Autosomal Recessive 14 0.034
472
BSC001 Buschke-Ollendorff Syndrome 59 0.034
473
ACR058 Acrofacial Dysostosis 1, Nager Type 39 0.034
474
LTH002 Lathosterolosis 29 0.034
475
c ATL002 Atelosteogenesis Ii 34 0.034
476
c CWD006 Cowden Syndrome 1 43 0.034
477
SMT001 Somatization Disorder 44 0.033
478
P NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 53 0.033
479
MHR002 Mohr Syndrome 29 0.033
480
URT016 Urethral Diverticulum 31 0.033
481
NCR003 Necrotizing Sialometaplasia 35 0.033
482
CHR399 Chromosome 4q21 Deletion Syndrome 22 0.032
483
PLL008 Pallister-Killian Syndrome 32 0.032
484
BRC097 Brachycephaly, Deafness, Cataract, Microstomia, and Mental Retardation 22 0.032
485
RNS001 Raine Syndrome 39 0.032
486
2Q3005 2q31.1 Microdeletion Syndrome 17 0.032
487
HNN001 Hennekam Syndrome 48 0.032
488
P DNT009 Dentin Dysplasia 37 0.031
489
CHR543 Chromosome 2q37 Deletion Syndrome 30 0.031
490
c ORF037 Orofaciodigital Syndrome I 43 0.031
491
c LRS002 Larsen-Like Syndrome 38 0.031
492
OHD004 Ohdo Syndrome 33 0.031
493
FRN012 Frontometaphyseal Dysplasia 37 0.031
494
TNS004 Tonsil Cancer 42 0.031
495
RVL002 Ruvalcaba Syndrome 32 0.031
496
MNT231 Mental Retardation, X-Linked Syndromic, Nascimento-Type 25 0.031
497
FNT003 Fountain Syndrome 26 0.031
498
CHR386 Chromosome 6pter-P24 Deletion Syndrome 23 0.030
499
HJD001 Hajdu-Cheney Syndrome 60 0.030
500
ONC003 Oncogenic Osteomalacia 40 0.030
501
LPR018 Leprechaunism 59 0.030
502
PLY056 Polyposis, Juvenile Intestinal 54 0.030
503
ECZ002 Eczema Herpeticum 46 0.030
504
P CNG046 Congenital Fiber-Type Disproportion 49 0.029
505
SPN113 Spinocerebellar Ataxia with Dysmorphism 17 0.029
506
BLR027 Blue Rubber Bleb Nevus 33 0.029
507
P KLN006 Koolen-De Vries Syndrome 38 0.029
508
c MNT109 Mental Retardation, X-Linked, Syndromic 15 30 0.029
509
CHR105 Choreoacanthocytosis 45 0.029
510
PRG123 Progeroid Syndrome, Neonatal 23 0.028
511
PRP082 Porphyria, Congenital Erythropoietic 44 0.028
512
ANT057 Antley-Bixler Syndrome Without Genital Anomalies or Disordered Steroidogenesis 28 0.028
513
CHR224 Chromosome 1q Duplication 21 0.028
514
CHR212 Chromosome 18p Duplication 19 0.028
515
CHN050 Chondrodysplasia with Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, and Microphthalmia 22 0.028
516
P FTL009 Fetal Akinesia Deformation Sequence 51 0.028
517
MSM004 Mesomelia-Synostoses Syndrome 24 0.027
518
SPR038 Supranuclear Ocular Palsy 20 0.027
519
PSD046 Pseudotrisomy 13 Syndrome 24 0.027
520
PPL003 Papillary Cystadenocarcinoma 36 0.027
521
SCH071 Schaaf-Yang Syndrome 26 0.027
522
CHR229 Chromosome 20p Duplication 19 0.027
523
c ORF035 Orofaciodigital Syndrome Iv 28 0.026
524
c GLP003 Geleophysic Dysplasia 1 26 0.026
525
MCR308 Microcephalic Primordial Dwarfism, Toriello Type 17 0.026
526
8Q1001 8q12 Microduplication Syndrome 12 0.026
527
c CRN134 Cornelia De Lange Syndrome 2 26 0.026
528
20P001 20p12.3 Microdeletion Syndrome 13 0.026
529
P OTP001 Otopalatodigital Syndrome 26 0.026
530
CHM006 Chime Syndrome 32 0.026
531
MCR063 Microcephaly, Holoprosencephaly, and Intrauterine Growth Retardation 7 0.026
532
c CRN209 Cornelia De Lange Syndrome 5 23 0.025
533
c FBR029 Fibrochondrogenesis 1 18 0.025
534
MMS001 Momo Syndrome 23 0.025
535
WLS004 Wilson-Turner Syndrome 31 0.024
536
P EHL025 Ehlers-Danlos Syndrome, Musculocontractural Type 33 0.024
537
SPN141 Spondyloepiphyseal Dysplasia-Brachydactyly and Distinctive Speech 15 0.024
538
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 26 0.024
539
GRC002 Gracile Bone Dysplasia 27 0.024
540
MNT121 Mental Retardation, X-Linked Syndromic, Christianson Type 23 0.023
541
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 23 0.023
542
CHR382 Chromosome 18q Deletion Syndrome 31 0.023
543
CHN043 Chondrodysplasia with Joint Dislocations, Grapp Type 20 0.023
544
SCH031 Scholte Syndrome 18 0.022
545
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 12 0.022
546
DPL009 Duplication of the Pituitary Gland 16 0.021
547
8PN001 8p Inverted Duplication/deletion Syndrome 12 0.021