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"

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

# Family MCID Name MIFTS Score
1
c CTR113 Cataract 11, Multiple Types 29 6.522
2
P CTR002 Cataract 57 0.713
3
RTN023 Retinitis 49 0.288
4
END072 Endotheliitis 42 0.279
5
EYD002 Eye Disease 63 0.242
6
ETH011 Ethylmalonic Encephalopathy 59 0.235
7
NRN002 Neuronitis 42 0.218
8
P HPT021 Hepatitis 70 0.216
9
CRB009 Cerebritis 38 0.213
10
GLB003 Globe Disease 35 0.208
11
P ENC018 Encephalopathy 59 0.199
12
AYM001 Ayme-Gripp Syndrome 45 0.190
13
P ART022 Arthritis 75 0.189
14
P LKM002 Leukemia 70 0.186
15
ALR002 Al-Raqad Syndrome 36 0.177
16
P NRP001 Neuropathy 60 0.176
17
P CRV039 Cervicitis 44 0.172
18
P MYC007 Myocardial Infarction 79 0.162
19
AST006 Astigmatism 44 0.159
20
P OBS005 Obesity 93 0.157
21
PRS047 Prostatitis 56 0.157
22
ADL002 Adult Syndrome 53 0.152
23
P PNC044 Pancreatitis 60 0.148
24
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.146
25
P LYM118 Lymphoma 70 0.145
26
P RHM011 Rheumatoid Arthritis 88 0.144
27
RTN018 Retinal Disease 56 0.143
28
ALN001 Aland Island Eye Disease 45 0.139
29
EXF001 Exfoliation Syndrome 57 0.134
30
P THY032 Thyroiditis 54 0.134
31
HNM002 Hinman Syndrome 25 0.131
32
P EPL164 Epilepsy 66 0.131
33
ADM013 Adamantinoma of Long Bones 59 0.131
34
P SCL015 Scleritis 49 0.131
35
P MYP004 Myopathy 67 0.130
36
DMN002 Dementia 64 0.129
37
P MYP006 Myopia 59 0.127
38
ISC004 Ischemia 59 0.123
39
P RTN008 Retinitis Pigmentosa 79 0.120
40
P HRT032 Heart Disease 76 0.119
41
P ART023 Arthropathy 63 0.114
42
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.111
43
P RTN016 Retinal Degeneration 54 0.110
44
P PRS040 Prostate Cancer 89 0.109
45
P INF032 Infertility 61 0.109
46
P NRV007 Nervous System Disease 71 0.108
47
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.108
48
KDS001 Kid Syndrome 53 0.106
49
CHL071 Child Syndrome 58 0.105
50
c CTR130 Cataract 9, Multiple Types 37 0.105
51
ANR002 Aniridia 60 0.104
52
P LPR003 Leprosy 68 0.102
53
ALL026 Allergic Hypersensitivity Disease 53 0.102
54
FST001 Foster-Kennedy Syndrome 34 0.100
55
RHM027 Rheumatic Disease 57 0.099
56
BRT030 Birth Defects 43 0.099
57
JNT002 Joint Disorders 56 0.098
58
OCL006 Ocular Hypertension 48 0.097
59
ACR041 Acromelic Frontonasal Dysostosis 46 0.097
60
P MSC005 Muscular Dystrophy 64 0.096
61
P KRT007 Keratoconus 51 0.096
62
OPT006 Optic Nerve Disease 51 0.095
63
ATH003 Atherosclerosis 62 0.095
64
BRN106 Burns 52 0.095
65
ATN002 Autonomic Nervous System Disease 47 0.093
66
P THR014 Thrombocytopenia 64 0.093
67
CTS003 Coats Disease 57 0.093
68
P CNJ013 Conjunctivitis 65 0.092
69
CNN005 Connective Tissue Disease 61 0.092
70
MTH009 Mouth Disease 63 0.092
71
P ESP024 Esophagitis 62 0.091
72
CYS001 Cystic Fibrosis 86 0.091
73
TBR010 Tuberculosis 69 0.091
74
STR067 Stroke, Ischemic 77 0.090
75
P GLM045 Glioma 58 0.090
76
DWR001 Dwarfism 46 0.090
77
NSD001 Nose Disease 52 0.090
78
PCK002 Pick Disease 67 0.089
79
EYD001 Eye Degenerative Disease 31 0.089
80
MVM001 Movement Disease 54 0.089
81
MSC004 Muscle Tissue Disease 36 0.088
82
P TRT010 Teratoma 52 0.088
83
P CRN026 Corneal Edema 40 0.088
84
P MSC033 Muscle Disorders 52 0.087
85
PRP027 Peripheral Vascular Disease 69 0.086
86
P DBT005 Diabetes Insipidus 53 0.084
87
NRL016 Neural Tube Defects 76 0.084
88
P INT068 Intestinal Disease 61 0.084
89
P ALZ034 Alzheimer Disease 93 0.083
90
P STR020 Strabismus 53 0.082
91
RNL007 Renal Tubular Acidosis 50 0.082
92
P HRP006 Herpes Simplex 65 0.081
93
c CNT035 Central Nervous System Disease 59 0.081
94
PRT037 Pertussis 64 0.081
95
NNC002 Nance-Horan Syndrome 36 0.080
96
LPD008 Lipid Metabolism Disorder 58 0.078
97
P PHC003 Pheochromocytoma 71 0.078
98
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.077
99
P ENC004 Encephalitis 61 0.077
100
P SPS003 Spastic Diplegia 53 0.076
101
P RTN024 Retinoblastoma 75 0.076
102
HRP004 Herpes Zoster 56 0.076
103
RDN001 Reading Disorder 39 0.075
104
P AMY004 Amyloidosis 64 0.074
105
ADT003 Auditory System Disease 51 0.074
106
ANX002 Anxiety Disorder 69 0.073
107
ALB002 Albinism 43 0.072
108
LRN003 Learning Disability 51 0.072
109
ALP008 Alopecia 55 0.071
110
GRW007 Growth Hormone Deficiency 48 0.071
111
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.070
112
P CRN178 Coronary Heart Disease 6 24 0.070
113
SPC010 Speech and Communication Disorders 46 0.069
114
c CHR089 Chronic Kidney Failure 66 0.069
115
P ANT026 Anterior Segment Mesenchymal Dysgenesis 38 0.068
116
DNT012 Dental Caries 46 0.068
117
P HMC003 Hemochromatosis 72 0.068
118
P MCP010 Mucopolysaccharidosis 58 0.068
119
HYP066 Hyperglycemia 60 0.067
120
P MCR129 Microvascular Complications of Diabetes 1 57 0.067
121
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.066
122
PRM097 Primary Immunodeficiency Disease 61 0.065
123
P THL005 Thalassemia 61 0.065
124
P END033 Endocarditis 52 0.065
125
CNG034 Congestive Heart Failure 71 0.064
126
ART021 Arteriosclerosis 59 0.062
127
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.061
128
NRT004 Neuritis 52 0.061
129
SKN023 Skin Tag 46 0.060
130
BRN071 Brain Injury 52 0.060
131
VSC006 Vascular Cancer 54 0.059
132
GLC003 Glucose Intolerance 55 0.058
133
ADR009 Adrenal Cortex Disease 41 0.058
134
CHR081 Choroideremia 53 0.058
135
P RFS001 Refsum Disease 62 0.057
136
c LBR014 Leber Congenital Amaurosis 4 47 0.057
137
PLY024 Polymicrogyria 36 0.057
138
CNR002 Cone-Rod Dystrophy 68 0.056
139
APH002 Aphasia 53 0.055
140
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.055
141
P CRN035 Cranial Nerve Palsy 43 0.055
142
CHR005 Chorioamnionitis 48 0.053
143
WLS001 Wilson Disease 72 0.053
144
ESP021 Esophageal Cancer 75 0.052
145
CRN031 Cranial Nerve Disease 40 0.052
146
MNN009 Meningoencephalitis 45 0.052
147
P NGH001 Night Blindness 49 0.051
148
c CHR417 Chronic Graft Versus Host Disease 50 0.051
149
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.049
150
HYD002 Hydronephrosis 47 0.049
151
URN010 Urinary Tract Obstruction 56 0.049
152
CYS010 Cystinosis 51 0.048
153
P MSC007 Muscle Hypertrophy 59 0.047
154
P STR022 Stargardt Disease 54 0.045
155
CRV043 Cervical Dystonia 44 0.042
156
FND002 Fundus Dystrophy 46 0.042
157
SPH010 Sphingolipidosis 45 0.040
158
c STR084 Stargardt Disease 1 52 0.038
159
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.038
160
STR046 Stargardt Macular Degeneration 29 0.038
161
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 35 0.037