Search results for "cataract, posterior polar, 4, syndromic"

The MalaCard for "cataract, posterior polar, 4, syndromic" has been retired.
Searching MalaCards for entries containing "cataract, posterior polar, 4, syndromic"

164 hits were found for 'cataract, posterior polar, 4, syndromic'

# Family MCID Name MIFTS Score
1
c CTR113 Cataract 11, Multiple Types 28 5.971
2
P CTR002 Cataract 57 0.726
3
RTN023 Retinitis 49 0.301
4
END072 Endotheliitis 41 0.282
5
AYM001 Ayme-Gripp Syndrome 40 0.252
6
ALR002 Al-Raqad Syndrome 36 0.239
7
NRN002 Neuronitis 40 0.228
8
CRB009 Cerebritis 36 0.224
9
P HPT021 Hepatitis 74 0.221
10
P ENC018 Encephalopathy 59 0.210
11
GLB003 Globe Disease 34 0.192
12
P LKM002 Leukemia 70 0.191
13
P ART022 Arthritis 73 0.190
14
P NRP001 Neuropathy 57 0.188
15
P CRV039 Cervicitis 45 0.176
16
MLN008 Melanoma 61 0.169
17
P OBS005 Obesity 91 0.167
18
PRS047 Prostatitis 56 0.162
19
P MYC007 Myocardial Infarction 80 0.161
20
AST006 Astigmatism 42 0.155
21
P RHM011 Rheumatoid Arthritis 87 0.153
22
P LYM118 Lymphoma 68 0.149
23
P PNC044 Pancreatitis 62 0.148
24
RTN018 Retinal Disease 55 0.148
25
P MYP004 Myopathy 67 0.143
26
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.143
27
P THY032 Thyroiditis 57 0.142
28
P EPL164 Epilepsy 60 0.141
29
ADL002 Adult Syndrome 53 0.140
30
P SCL015 Scleritis 49 0.140
31
ALN001 Aland Island Eye Disease 45 0.137
32
P KDN018 Kidney Disease 64 0.137
33
P MYP006 Myopia 58 0.136
34
DMN002 Dementia 62 0.136
35
EXF001 Exfoliation Syndrome 56 0.135
36
P RTN008 Retinitis Pigmentosa 78 0.133
37
ADM013 Adamantinoma of Long Bones 57 0.132
38
P NPH012 Nephrotic Syndrome 55 0.128
39
ISC004 Ischemia 56 0.127
40
ACQ007 Acquired Immunodeficiency Syndrome 60 0.124
41
P NRV007 Nervous System Disease 71 0.123
42
P ART023 Arthropathy 63 0.123
43
P AST005 Asthma 80 0.119
44
c CTR130 Cataract 9, Multiple Types 36 0.114
45
P PRS040 Prostate Cancer 89 0.112
46
P INF032 Infertility 61 0.112
47
P LPR003 Leprosy 70 0.111
48
c CNG401 Congenital Heart Disease 67 0.110
49
RHM027 Rheumatic Disease 55 0.109
50
ANR002 Aniridia 62 0.108
51
P MSC005 Muscular Dystrophy 64 0.105
52
KDS001 Kid Syndrome 53 0.105
53
DWR001 Dwarfism 42 0.105
54
BRT030 Birth Defects 44 0.104
55
P RTN016 Retinal Degeneration 50 0.104
56
CHL071 Child Syndrome 58 0.104
57
BRN106 Burns 52 0.103
58
ACR041 Acromelic Frontonasal Dysostosis 45 0.102
59
TBR010 Tuberculosis 70 0.102
60
NRL016 Neural Tube Defects 76 0.102
61
P ESP024 Esophagitis 62 0.101
62
JNT002 Joint Disorders 55 0.101
63
FST001 Foster-Kennedy Syndrome 31 0.101
64
P KRT007 Keratoconus 48 0.100
65
ATH003 Atherosclerosis 63 0.100
66
OCL006 Ocular Hypertension 47 0.099
67
P THR014 Thrombocytopenia 63 0.099
68
ALL026 Allergic Hypersensitivity Disease 53 0.099
69
OPT006 Optic Nerve Disease 47 0.097
70
CNN005 Connective Tissue Disease 60 0.096
71
ATN002 Autonomic Nervous System Disease 46 0.096
72
P HRT032 Heart Disease 64 0.096
73
P TRT010 Teratoma 49 0.096
74
CYS001 Cystic Fibrosis 87 0.095
75
NTR005 Nutritional Deficiency Disease 51 0.095
76
P CNJ013 Conjunctivitis 65 0.095
77
P ALZ034 Alzheimer Disease 92 0.094
78
P CRN026 Corneal Edema 39 0.093
79
P DBT005 Diabetes Insipidus 53 0.092
80
P MSC033 Muscle Disorders 52 0.092
81
CTS003 Coats Disease 57 0.092
82
MTH009 Mouth Disease 63 0.092
83
KRT001 Keratoconjunctivitis Sicca 58 0.091
84
MVM001 Movement Disease 45 0.091
85
P GLM045 Glioma 53 0.090
86
RNL007 Renal Tubular Acidosis 50 0.089
87
EYD001 Eye Degenerative Disease 31 0.089
88
PRT037 Pertussis 63 0.089
89
PCK002 Pick Disease 66 0.088
90
NSD001 Nose Disease 51 0.088
91
P INT068 Intestinal Disease 60 0.088
92
PRP027 Peripheral Vascular Disease 69 0.088
93
P STR020 Strabismus 55 0.087
94
SPN051 Spondylitis 50 0.086
95
P HRP006 Herpes Simplex 65 0.086
96
P PLY019 Polyneuropathy 53 0.085
97
TTN003 Tetanus 62 0.084
98
MSC004 Muscle Tissue Disease 35 0.084
99
P ENC004 Encephalitis 60 0.084
100
SYN007 Synovitis 56 0.084
101
P PHC003 Pheochromocytoma 72 0.083
102
HRP004 Herpes Zoster 56 0.083
103
P BRN009 Burning Mouth Syndrome 54 0.082
104
SKN016 Skin Disease 69 0.081
105
c CNT035 Central Nervous System Disease 60 0.081
106
NNC002 Nance-Horan Syndrome 37 0.078
107
P AMY004 Amyloidosis 63 0.078
108
ALB002 Albinism 43 0.078
109
ALP008 Alopecia 56 0.077
110
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.077
111
P SPS003 Spastic Diplegia 49 0.077
112
P RTN024 Retinoblastoma 75 0.077
113
P HMC003 Hemochromatosis 71 0.076
114
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.075
115
ADT003 Auditory System Disease 49 0.075
116
RDN001 Reading Disorder 39 0.075
117
P MYC008 Myocarditis 56 0.074
118
LRN003 Learning Disability 49 0.074
119
CNR002 Cone-Rod Dystrophy 65 0.074
120
c CHR089 Chronic Kidney Failure 67 0.072
121
GLC003 Glucose Intolerance 56 0.072
122
FML039 Female Reproductive System Disease 49 0.072
123
VSC007 Vascular Disease 51 0.072
124
DNT012 Dental Caries 45 0.072
125
CND005 Cone Dystrophy 37 0.072
126
HYP066 Hyperglycemia 61 0.072
127
P END033 Endocarditis 52 0.072
128
ANX002 Anxiety Disorder 67 0.071
129
c MCR129 Microvascular Complications of Diabetes 1 55 0.070
130
P ANT026 Anterior Segment Mesenchymal Dysgenesis 36 0.070
131
ART021 Arteriosclerosis 59 0.070
132
P THL005 Thalassemia 61 0.069
133
P CRN178 Coronary Heart Disease 6 22 0.069
134
SPC010 Speech and Communication Disorders 42 0.069
135
NRT004 Neuritis 52 0.069
136
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.068
137
P MCP010 Mucopolysaccharidosis 58 0.068
138
CHR081 Choroideremia 53 0.068
139
BRN024 Bronchitis 67 0.068
140
c LBR014 Leber Congenital Amaurosis 4 41 0.067
141
P NGH001 Night Blindness 49 0.066
142
CNG034 Congestive Heart Failure 72 0.066
143
BRN071 Brain Injury 51 0.066
144
PLY024 Polymicrogyria 34 0.062
145
P GST044 Gastritis 64 0.062
146
ADR009 Adrenal Cortex Disease 40 0.062
147
APH002 Aphasia 52 0.062
148
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.061
149
MNN009 Meningoencephalitis 42 0.060
150
WLS001 Wilson Disease 72 0.059
151
P STR022 Stargardt Disease 48 0.058
152
ESP021 Esophageal Cancer 75 0.057
153
FND002 Fundus Dystrophy 46 0.056
154
P CRN035 Cranial Nerve Palsy 44 0.056
155
HYD002 Hydronephrosis 48 0.056
156
CRN031 Cranial Nerve Disease 39 0.053
157
c CHR417 Chronic Graft Versus Host Disease 50 0.052
158
P MSC007 Muscle Hypertrophy 55 0.051
159
CYS010 Cystinosis 51 0.051
160
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 41 0.050
161
STR046 Stargardt Macular Degeneration 27 0.048
162
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.048
163
SPH010 Sphingolipidosis 44 0.047
164
CRV043 Cervical Dystonia 43 0.047