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"

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

# Family MCID Name MIFTS Score
1
c CTR113 Cataract 11, Multiple Types 31 6.632
2
P CTR002 Cataract 58 0.665
3
RTN023 Retinitis 50 0.282
4
END072 Endotheliitis 42 0.273
5
EYD002 Eye Disease 61 0.227
6
ETH011 Ethylmalonic Encephalopathy 56 0.220
7
P HPT021 Hepatitis 69 0.214
8
NRN002 Neuronitis 41 0.214
9
CRB009 Cerebritis 39 0.209
10
GLB003 Globe Disease 32 0.199
11
P ENC018 Encephalopathy 59 0.196
12
P LKM002 Leukemia 71 0.182
13
P ART022 Arthritis 75 0.179
14
ALR002 Al-Raqad Syndrome 36 0.173
15
P NRP001 Neuropathy 59 0.171
16
P CRV039 Cervicitis 45 0.169
17
MLN008 Melanoma 62 0.162
18
P MYC007 Myocardial Infarction 79 0.159
19
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.158
20
P OBS005 Obesity 92 0.156
21
PRS047 Prostatitis 56 0.152
22
AST006 Astigmatism 45 0.151
23
ADL002 Adult Syndrome 52 0.145
24
P PNC044 Pancreatitis 61 0.144
25
P LYM118 Lymphoma 69 0.144
26
HNM002 Hinman Syndrome 25 0.140
27
HPT074 Hepatic Adenoma, Somatic 50 0.140
28
P RHM011 Rheumatoid Arthritis 89 0.140
29
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.139
30
ISC004 Ischemia 61 0.136
31
RTN018 Retinal Disease 53 0.133
32
P THY032 Thyroiditis 54 0.131
33
P EPL164 Epilepsy 66 0.130
34
P KDN018 Kidney Disease 66 0.129
35
ALN001 Aland Island Eye Disease 45 0.127
36
DMN002 Dementia 65 0.126
37
ADM013 Adamantinoma of Long Bones 57 0.126
38
EXF001 Exfoliation Syndrome 57 0.126
39
P SCL015 Scleritis 49 0.126
40
P MYP004 Myopathy 67 0.124
41
P MYP006 Myopia 56 0.123
42
P NPH012 Nephrotic Syndrome 59 0.120
43
c HPT001 Hepatitis C 68 0.118
44
P RTN008 Retinitis Pigmentosa 80 0.117
45
P INF038 Influenza 72 0.113
46
P HRT032 Heart Disease 75 0.113
47
P ART023 Arthropathy 64 0.111
48
P FNC043 Fanconi Anemia, Complementation Group E 55 0.109
49
P PRS040 Prostate Cancer 90 0.108
50
P NRV007 Nervous System Disease 71 0.107
51
P INF032 Infertility 59 0.105
52
KDS001 Kid Syndrome 53 0.104
53
P RTN016 Retinal Degeneration 54 0.104
54
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.104
55
ACQ007 Acquired Immunodeficiency Syndrome 60 0.103
56
CHL071 Child Syndrome 58 0.102
57
FST001 Foster-Kennedy Syndrome 31 0.099
58
ALL026 Allergic Hypersensitivity Disease 52 0.098
59
P LPR003 Leprosy 69 0.098
60
P ANR002 Aniridia 64 0.097
61
c CTR130 Cataract 9, Multiple Types 37 0.097
62
P LVR013 Liver Disease 75 0.097
63
JNT002 Joint Disorders 55 0.096
64
SQM006 Squamous Cell Carcinoma 70 0.096
65
BRT030 Birth Defects 43 0.096
66
OPT006 Optic Nerve Disease 52 0.096
67
ACR041 Acromelic Frontonasal Dysostosis 45 0.096
68
RHM027 Rheumatic Disease 58 0.095
69
AYM001 Ayme-Gripp Syndrome 41 0.095
70
SPN369 Spinal Disease 39 0.094
71
P KRT007 Keratoconus 48 0.094
72
P MSC005 Muscular Dystrophy 65 0.094
73
ATH003 Atherosclerosis 65 0.094
74
ADN018 Adenoma 58 0.092
75
OCL006 Ocular Hypertension 48 0.092
76
NRM005 Neuromuscular Disease 56 0.092
77
PRP027 Peripheral Vascular Disease 69 0.092
78
BRN106 Burns 52 0.090
79
MTH009 Mouth Disease 61 0.090
80
DWR001 Dwarfism 47 0.090
81
CYS001 Cystic Fibrosis 83 0.089
82
MSC004 Muscle Tissue Disease 34 0.089
83
CTS003 Coats Disease 57 0.089
84
P ESP024 Esophagitis 61 0.089
85
P GLM045 Glioma 60 0.089
86
ATN002 Autonomic Nervous System Disease 48 0.088
87
P CNJ013 Conjunctivitis 64 0.088
88
P TRT010 Teratoma 52 0.087
89
NSD001 Nose Disease 48 0.087
90
c HPT016 Hepatitis B 65 0.086
91
PCK002 Pick Disease 68 0.086
92
MVM001 Movement Disease 49 0.086
93
P INF037 Inflammatory Bowel Disease 63 0.086
94
STR067 Stroke, Ischemic 75 0.086
95
NRL016 Neural Tube Defects 76 0.086
96
EYD001 Eye Degenerative Disease 30 0.086
97
PRP030 Purpura 58 0.085
98
P CRN026 Corneal Edema 42 0.085
99
GLC008 Glucose Metabolism Disease 42 0.083
100
c HPT003 Hepatitis a 59 0.082
101
LPD008 Lipid Metabolism Disorder 58 0.082
102
RNL007 Renal Tubular Acidosis 50 0.081
103
P ALZ034 Alzheimer Disease 92 0.080
104
P STR020 Strabismus 51 0.080
105
P DBT005 Diabetes Insipidus 53 0.079
106
P INT068 Intestinal Disease 60 0.079
107
PRT037 Pertussis 64 0.079
108
P HRP006 Herpes Simplex 65 0.078
109
ADT003 Auditory System Disease 40 0.078
110
c CNT035 Central Nervous System Disease 60 0.078
111
P ENC004 Encephalitis 63 0.077
112
P PLY006 Polydactyly 56 0.076
113
P AMY004 Amyloidosis 65 0.075
114
NNC002 Nance-Horan Syndrome 37 0.075
115
c CTR141 Cataract 21, Multiple Types 37 0.075
116
RDN001 Reading Disorder 34 0.075
117
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.074
118
P EPN002 Ependymoma 53 0.074
119
P RTN024 Retinoblastoma 74 0.074
120
ANX002 Anxiety Disorder 67 0.073
121
LRN003 Learning Disability 49 0.072
122
HRP004 Herpes Zoster 56 0.072
123
P SPS003 Spastic Diplegia 52 0.072
124
GRW007 Growth Hormone Deficiency 50 0.071
125
c TRC078 Trichohepatoenteric Syndrome 2 29 0.071
126
ALB002 Albinism 46 0.071
127
CNG034 Congestive Heart Failure 72 0.070
128
ALP008 Alopecia 57 0.069
129
SYN007 Synovitis 58 0.069
130
MSL001 Measles 61 0.069
131
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.068
132
ART021 Arteriosclerosis 58 0.068
133
GST050 Gastrointestinal System Disease 56 0.068
134
SPC010 Speech and Communication Disorders 41 0.067
135
P HMC003 Hemochromatosis 72 0.066
136
c HYP595 Hypertension, Essential 69 0.066
137
P MCP010 Mucopolysaccharidosis 60 0.066
138
P THL005 Thalassemia 64 0.066
139
P PHC003 Pheochromocytoma 71 0.065
140
P END033 Endocarditis 54 0.065
141
P MSC003 Muscular Atrophy 50 0.065
142
END030 End Stage Renal Failure 55 0.063
143
P GT001 Gout 58 0.063
144
P MCR129 Microvascular Complications of Diabetes 1 54 0.063
145
P APL001 Aplastic Anemia 75 0.063
146
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.062
147
P OST028 Osteochondroma 47 0.062
148
GGN002 Gigantism 32 0.061
149
GLC003 Glucose Intolerance 55 0.060
150
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.059
151
SKN023 Skin Tag 44 0.059
152
ADR009 Adrenal Cortex Disease 39 0.058
153
BRN071 Brain Injury 52 0.058
154
c CLL013 Cell Type Cancer 46 0.058
155
APR001 Apraxia 51 0.057
156
MTR014 Motor Neuron Disease 58 0.056
157
P SPN046 Spinal Muscular Atrophy 65 0.056
158
PLY024 Polymicrogyria 35 0.055
159
CHR081 Choroideremia 54 0.055
160
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.055
161
APH002 Aphasia 54 0.054
162
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.054
163
P CRN035 Cranial Nerve Palsy 46 0.053
164
HDN002 Head Injury 45 0.052
165
NNL002 Nonalcoholic Steatohepatitis 50 0.052
166
WLS001 Wilson Disease 72 0.051
167
ESP021 Esophageal Cancer 76 0.051
168
CRN031 Cranial Nerve Disease 40 0.051
169
FCL011 Facial Nerve Disease 36 0.051
170
P LKD001 Leukodystrophy 59 0.050
171
GNC005 Geniculate Ganglionitis 27 0.049
172
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.049
173
CYS010 Cystinosis 53 0.046
174
P HYP076 Hyperthyroidism 55 0.046
175
P MSC007 Muscle Hypertrophy 58 0.045
176
P ANT026 Anterior Segment Mesenchymal Dysgenesis 42 0.044
177
c SPN318 Spinal Muscular Atrophy-4 35 0.044
178
c PRG001 Progressive Muscular Atrophy 39 0.042
179
CRV043 Cervical Dystonia 44 0.041
180
SYS003 Systolic Heart Failure 43 0.039
181
c SPN315 Spinal Muscular Atrophy-1 47 0.037
182
c SPN317 Spinal Muscular Atrophy-3 39 0.037
183
c ADL016 Adult Spinal Muscular Atrophy 31 0.036
184
c JVN006 Juvenile Spinal Muscular Atrophy 34 0.036
185
SRV001 Survival Motor Neuron Spinal Muscular Atrophy 25 0.036
186
PRX014 Proximal Spinal Muscular Atrophy 36 0.036
187
c SPN316 Spinal Muscular Atrophy-2 42 0.034