Search results for cataract, posterior polar, 4, syndromic

185 hits were found for cataract, posterior polar, 4, syndromic

# Family MCID Name MIFTS Score
1
c CTR113 Cataract 11, Multiple Types 32 6.641
2
P CTR002 Cataract 57 0.655
3
RTN023 Retinitis 49 0.288
4
END072 Endotheliitis 41 0.272
5
EYD002 Eye Disease 57 0.252
6
CRB009 Cerebritis 39 0.214
7
NRN002 Neuronitis 39 0.213
8
P HPT021 Hepatitis 68 0.211
9
P ART022 Arthritis 72 0.200
10
ADL002 Adult Syndrome 57 0.185
11
P LKM002 Leukemia 72 0.185
12
P CRV039 Cervicitis 45 0.179
13
P NRP001 Neuropathy 57 0.173
14
MLN008 Melanoma 70 0.169
15
P BRS047 Breast Cancer 100 0.166
16
P MYC007 Myocardial Infarction 77 0.166
17
P OBS005 Obesity 91 0.166
18
PRS047 Prostatitis 55 0.157
19
ALR002 Al-Raqad Syndrome 29 0.154
20
AST006 Astigmatism 43 0.151
21
P LYM118 Lymphoma 69 0.149
22
HPT074 Hepatic Adenoma, Somatic 44 0.147
23
NLL002 Null Syndrome 26 0.147
24
P PNC044 Pancreatitis 60 0.144
25
P KDN018 Kidney Disease 65 0.144
26
ISC004 Ischemia 59 0.141
27
HNM002 Hinman Syndrome 27 0.140
28
P RHM011 Rheumatoid Arthritis 87 0.137
29
BRT030 Birth Defects 44 0.136
30
P ART023 Arthropathy 62 0.135
31
P THY032 Thyroiditis 53 0.133
32
CHR008 Choroiditis 43 0.130
33
P EPL164 Epilepsy 65 0.130
34
P AST005 Asthma 81 0.128
35
P NRV007 Nervous System Disease 70 0.127
36
P SCL015 Scleritis 46 0.127
37
DMN002 Dementia 52 0.126
38
EXF001 Exfoliation Syndrome 57 0.126
39
P NPH012 Nephrotic Syndrome 59 0.126
40
P MYP006 Myopia 59 0.125
41
JNT002 Joint Disorders 55 0.123
42
RTN018 Retinal Disease 51 0.123
43
P HYP729 Hypersensitivity Reaction Disease 43 0.120
44
ACQ007 Acquired Immunodeficiency Syndrome 60 0.119
45
RHM027 Rheumatic Disease 57 0.119
46
P RTN008 Retinitis Pigmentosa 80 0.118
47
MTH009 Mouth Disease 62 0.117
48
P RTN016 Retinal Degeneration 53 0.117
49
P INF032 Infertility 57 0.111
50
P PRS040 Prostate Cancer 88 0.111
51
KDS001 Kid Syndrome 57 0.110
52
c CTR130 Cataract 9, Multiple Types 40 0.110
53
P HRT032 Heart Disease 75 0.110
54
CHL071 Child Syndrome 59 0.110
55
P FNC043 Fanconi Anemia, Complementation Group E 51 0.106
56
URN009 Urinary System Disease 49 0.105
57
P MYP004 Myopathy 68 0.105
58
IMM136 Immune System Disease 53 0.101
59
c HPT073 Hepatitis C Virus 70 0.101
60
P LPR003 Leprosy 63 0.101
61
ANX002 Anxiety Disorder 66 0.101
62
c CNT035 Central Nervous System Disease 60 0.101
63
P LPS004 Lupus Erythematosus 63 0.100
64
P LVR013 Liver Disease 72 0.099
65
P ANR002 Aniridia 66 0.099
66
PHY002 Physical Disorder 43 0.098
67
MSC004 Muscle Tissue Disease 37 0.098
68
SKN016 Skin Disease 64 0.097
69
ATH003 Atherosclerosis 65 0.097
70
P INT068 Intestinal Disease 59 0.096
71
c SYS001 Systemic Lupus Erythematosus 86 0.095
72
CNN005 Connective Tissue Disease 61 0.095
73
P MSC005 Muscular Dystrophy 65 0.095
74
SQM006 Squamous Cell Carcinoma 69 0.095
75
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.094
76
P MLT019 Multiple Myeloma 82 0.094
77
PCK002 Pick Disease 68 0.094
78
BRN106 Burns 52 0.094
79
P GLM045 Glioma 59 0.093
80
P KRT007 Keratoconus 48 0.093
81
HV1006 Hiv-1 80 0.092
82
ADN018 Adenoma 58 0.092
83
P HPT023 Hepatocellular Carcinoma 89 0.091
84
P MSC033 Muscle Disorders 52 0.090
85
VRL011 Viral Infectious Disease 59 0.090
86
CYS001 Cystic Fibrosis 86 0.090
87
c CTR141 Cataract 21, Multiple Types 38 0.090
88
TBR010 Tuberculosis 69 0.089
89
GST050 Gastrointestinal System Disease 53 0.089
90
P CNJ013 Conjunctivitis 63 0.088
91
OCL006 Ocular Hypertension 46 0.088
92
DWR001 Dwarfism 45 0.087
93
NRL016 Neural Tube Defects 76 0.086
94
P TRT010 Teratoma 51 0.086
95
CTS003 Coats Disease 58 0.085
96
VSC007 Vascular Disease 65 0.084
97
P CRN026 Corneal Edema 39 0.084
98
MVM001 Movement Disease 52 0.083
99
P SPS003 Spastic Diplegia 52 0.082
100
c HPT003 Hepatitis a 56 0.082
101
P DBT005 Diabetes Insipidus 52 0.081
102
P INF037 Inflammatory Bowel Disease 62 0.081
103
P STR020 Strabismus 52 0.081
104
ATN002 Autonomic Nervous System Disease 48 0.080
105
P ALZ034 Alzheimer Disease 76 0.080
106
RNL007 Renal Tubular Acidosis 48 0.077
107
PRT037 Pertussis 63 0.077
108
NNC002 Nance-Horan Syndrome 38 0.077
109
P ENC004 Encephalitis 61 0.077
110
P HRP006 Herpes Simplex 62 0.077
111
P EPN002 Ependymoma 53 0.077
112
HRP004 Herpes Zoster 54 0.075
113
P AMY004 Amyloidosis 64 0.074
114
c TRC078 Trichohepatoenteric Syndrome 2 34 0.073
115
P GLM007 Glomerulonephritis 55 0.073
116
SKN023 Skin Tag 46 0.073
117
P PHC003 Pheochromocytoma 72 0.072
118
P RTN024 Retinoblastoma 75 0.072
119
VGT001 Vogt-Koyanagi-Harada Disease 55 0.071
120
ALB002 Albinism 45 0.071
121
VND001 Vein Disease 49 0.070
122
CNG034 Congestive Heart Failure 70 0.070
123
P END033 Endocarditis 53 0.069
124
ALP008 Alopecia 54 0.068
125
MNT002 Mental Depression 52 0.068
126
PPL022 Papilloma 54 0.068
127
CND002 Conduct Disorder 53 0.066
128
GRW007 Growth Hormone Deficiency 48 0.066
129
END030 End Stage Renal Failure 51 0.065
130
P THL005 Thalassemia 61 0.064
131
NRT004 Neuritis 51 0.063
132
FBR054 Fibroma 41 0.062
133
P GST049 Gastrointestinal System Cancer 59 0.062
134
P GT001 Gout 55 0.061
135
P RTN025 Retinoschisis 57 0.061
136
BRN028 Brain Cancer 67 0.061
137
SNS023 Sensory System Cancer 44 0.059
138
P NSP012 Nasopharyngeal Carcinoma 66 0.059
139
NSD001 Nose Disease 49 0.057
140
EYD001 Eye Degenerative Disease 32 0.056
141
P ANT073 Anterior Segment Dysgenesis 1, Multiple Subtypes 40 0.056
142
APH002 Aphasia 55 0.055
143
GNG004 Ganglioglioma 49 0.055
144
PLY024 Polymicrogyria 36 0.055
145
CHR081 Choroideremia 54 0.054
146
RDN001 Reading Disorder 36 0.054
147
CRB039 Cerebrovascular Disease 63 0.054
148
OPT006 Optic Nerve Disease 49 0.054
149
CND005 Cone Dystrophy 38 0.053
150
ADR009 Adrenal Cortex Disease 39 0.053
151
c CHR417 Chronic Graft Versus Host Disease 50 0.051
152
URN010 Urinary Tract Obstruction 53 0.050
153
P MMP001 Mumps 54 0.050
154
SPN186 Spinal Cord Injury 62 0.049
155
HYD002 Hydronephrosis 46 0.048
156
MNN009 Meningoencephalitis 45 0.048
157
CRN031 Cranial Nerve Disease 41 0.048
158
c MTR002 Mitral Valve Insufficiency 45 0.047
159
P LBR001 Leber Congenital Amaurosis 62 0.047
160
CYS010 Cystinosis 53 0.046
161
P STR022 Stargardt Disease 56 0.046
162
CRB038 Cerebral Ventricle Cancer 32 0.045
163
P RNV001 Renovascular Hypertension 46 0.045
164
CRV043 Cervical Dystonia 43 0.044
165
MDL003 Medullomyoblastoma 35 0.044
166
TRN018 Transitional Cell Carcinoma 52 0.043
167
URN008 Urinary Bladder Cancer 63 0.043
168
SYS003 Systolic Heart Failure 43 0.043
169
P NGH001 Night Blindness 47 0.043
170
CNR007 Cone-Rod Dystrophy 6 47 0.043
171
WLS001 Wilson Disease 73 0.043
172
CRB040 Cerebrum Cancer 33 0.042
173
c NRV012 Nervous System Benign Neoplasm 30 0.041
174
c ACH021 Achromatopsia 3 45 0.040
175
SPR024 Supratentorial Cancer 33 0.039
176
GLM004 Gliomatosis Cerebri 49 0.039
177
c STR084 Stargardt Disease 1 52 0.039
178
CRV038 Cervical Squamous Cell Carcinoma 57 0.039
179
BLS003 Blastoma 37 0.039
180
CRB022 Cerebellar Liponeurocytoma 32 0.037
181
P ACH003 Achromatopsia 55 0.036
182
SPN040 Spinal Cancer 42 0.036
183
STR046 Stargardt Macular Degeneration 27 0.035
184
MLN004 Melanotic Medulloblastoma 22 0.034
185
c APL013 Aipl1-Related Leber Congenital Amaurosis 19 0.034
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