Search results for "unexplained intellectual disability"

The MalaCard for "unexplained intellectual disability" has been retired.
Searching MalaCards for entries containing "unexplained intellectual disability"

187 hits were found for 'unexplained intellectual disability'

# Family MCID Name MIFTS Score
1
P INT063 Intellectual Disability 49 0.566
2
LRN003 Learning Disability 49 0.228
3
P EPL164 Epilepsy 66 0.166
4
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.112
5
P OBS005 Obesity 92 0.111
6
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.100
7
c PND001 Pain Disorder 54 0.092
8
P CHR345 Chronic Pain 50 0.086
9
DSS008 Disease of Mental Health 52 0.086
10
P ENC018 Encephalopathy 59 0.082
11
CRB009 Cerebritis 39 0.082
12
ALR002 Al-Raqad Syndrome 36 0.082
13
P ATX004 Ataxia 53 0.080
14
CND002 Conduct Disorder 54 0.077
15
P SDD001 Sudden Infant Death Syndrome 61 0.076
16
P ART022 Arthritis 75 0.072
17
P CRV039 Cervicitis 45 0.072
18
KDS001 Kid Syndrome 53 0.072
19
ATS001 Autistic Disorder 63 0.071
20
P MYP004 Myopathy 67 0.071
21
PHY002 Physical Disorder 43 0.070
22
CHL071 Child Syndrome 58 0.069
23
P THR015 Thrombophilia 59 0.068
24
P CRD011 Cardiomyopathy 68 0.068
25
ACR041 Acromelic Frontonasal Dysostosis 45 0.067
26
PSY004 Psychotic Disorder 67 0.065
27
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.065
28
P MSC005 Muscular Dystrophy 65 0.065
29
BRT030 Birth Defects 43 0.065
30
THR024 Thrombosis 57 0.064
31
NTR005 Nutritional Deficiency Disease 36 0.064
32
P HRT032 Heart Disease 75 0.063
33
PRD011 Proud Syndrome 42 0.063
34
P SHR029 Short Syndrome 58 0.063
35
P DRR001 Diarrhea 60 0.062
36
P LKM002 Leukemia 71 0.062
37
P ATS049 Autism Susceptibility, X-Linked 2 33 0.061
38
NRM005 Neuromuscular Disease 56 0.061
39
P BRS047 Breast Cancer 100 0.060
40
P NRV007 Nervous System Disease 71 0.060
41
P NTR004 Neutropenia 59 0.060
42
P HPT021 Hepatitis 69 0.059
43
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.059
44
ANX002 Anxiety Disorder 67 0.058
45
BRN071 Brain Injury 52 0.057
46
P SZR006 Seizure Disorder 56 0.055
47
P CLR023 Colorectal Cancer 97 0.055
48
MDD011 Mood Disorder 61 0.054
49
CRB045 Cerebellar Hypoplasia 48 0.054
50
c CNT035 Central Nervous System Disease 60 0.053
51
P SPS003 Spastic Diplegia 52 0.052
52
RTN023 Retinitis 50 0.052
53
EXF001 Exfoliation Syndrome 57 0.052
54
P MSC033 Muscle Disorders 52 0.051
55
STR067 Stroke, Ischemic 75 0.051
56
c CNG031 Congenital Nervous System Abnormality 37 0.050
57
SBS003 Substance Abuse 54 0.050
58
P THY032 Thyroiditis 54 0.050
59
WLL006 Wells Syndrome 59 0.050
60
P VLC001 Velocardiofacial Syndrome 62 0.049
61
MNT002 Mental Depression 53 0.049
62
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.049
63
P AMY004 Amyloidosis 65 0.049
64
WST001 West Syndrome 57 0.049
65
SKN016 Skin Disease 66 0.048
66
P NRF002 Neurofibromatosis 71 0.048
67
P CLC005 Celiac Disease 68 0.048
68
P LYM118 Lymphoma 69 0.046
69
DYS073 Dysphagia 48 0.046
70
RBR001 Roberts Syndrome 60 0.046
71
P HYP040 Hypospadias 57 0.046
72
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.046
73
P CHR084 Chromosomal Disease 32 0.046
74
P INF038 Influenza 72 0.045
75
P HYD006 Hydrocephalus 66 0.045
76
CSY001 C Syndrome 50 0.044
77
END040 Endogenous Depression 53 0.044
78
P CLL015 Collagen Disease 50 0.044
79
GLB003 Globe Disease 32 0.043
80
VSC047 Vascular Malformation 45 0.043
81
ALX002 Alexithymia 37 0.043
82
c MNT149 Mental Retardation, X-Linked 3 29 0.043
83
MNK001 Menkes Disease 60 0.043
84
BHR001 Behr Syndrome 42 0.043
85
WDS002 Woods Syndrome 27 0.043
86
ATP002 Atopy 66 0.043
87
PRM025 Primary Bacterial Infectious Disease 41 0.043
88
P MYC007 Myocardial Infarction 79 0.041
89
P PRM019 Premature Ovarian Failure 64 0.041
90
DBT088 Diabetes Insipidus, Nephrogenic 56 0.041
91
GRN017 Granulocytopenia 44 0.041
92
P OST005 Osteogenesis Imperfecta 69 0.041
93
P PLY019 Polyneuropathy 56 0.041
94
PRC013 Pericarditis 51 0.040
95
CCN007 Cocoon Syndrome 45 0.040
96
GDS001 Good Syndrome 44 0.040
97
P ALC004 Alcohol Abuse 59 0.040
98
P DYS007 Dyskeratosis Congenita 63 0.039
99
c MNT223 Mental Retardation, X-Linked 100 19 0.039
100
P KDN018 Kidney Disease 66 0.038
101
HYP056 Hypoglycemia 61 0.038
102
SXD001 Sex Differentiation Disease 38 0.038
103
P HMR003 Hemorrhagic Disease 57 0.038
104
CNT098 Central Core Disease 65 0.038
105
P HRD018 Hair Disease 51 0.038
106
CLN019 Colonic Disease 51 0.038
107
NRM004 Neuroma 48 0.037
108
CNV002 Conversion Disorder 41 0.037
109
P ENC004 Encephalitis 63 0.037
110
HYP066 Hyperglycemia 61 0.037
111
STT001 Status Epilepticus 59 0.037
112
ATN005 Autonomic Dysfunction 49 0.037
113
P MNN013 Meningitis 67 0.035
114
P NRV006 Nervous System Cancer 60 0.035
115
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.035
116
NRF007 Neurofibroma 53 0.035
117
ADT003 Auditory System Disease 40 0.035
118
PRT014 Protein S Deficiency 53 0.035
119
HDG012 Hodgkin Lymphoma 77 0.035
120
c DLT002 Dilated Cardiomyopathy 76 0.035
121
P MLT074 Multiple Endocrine Neoplasia 56 0.035
122
P ANT006 Antiphospholipid Syndrome 56 0.035
123
P HYP097 Hyperekplexia 54 0.035
124
P GND004 Gonadal Dysgenesis 51 0.035
125
AMN001 Amenorrhea 50 0.035
126
FBR054 Fibroma 46 0.035
127
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.035
128
PRM013 Premature Menopause 41 0.035
129
P 3MT007 3-Methylglutaconic Aciduria 39 0.035
130
IRN004 Iron-Refractory Iron Deficiency Anemia 38 0.035
131
HMC014 Homocysteinemia 35 0.035
132
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.035
133
c EPL082 Epileptic Encephalopathy, Early Infantile, 13 19 0.035
134
P OST002 Osteoporosis 64 0.034
135
GLT021 Glutaricaciduria, Type I 46 0.034
136
ABL002 Ablepharon-Macrostomia Syndrome 57 0.032
137
c SYS001 Systemic Lupus Erythematosus 86 0.032
138
P LPS004 Lupus Erythematosus 64 0.032
139
P ORT004 Orthostatic Intolerance 64 0.032
140
P CTS001 Cutis Laxa 58 0.032
141
CTS003 Coats Disease 57 0.032
142
ADL002 Adult Syndrome 52 0.032
143
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.029
144
P PLY011 Polycystic Ovary Syndrome 65 0.029
145
WLM007 Wilms Tumor Susceptibility-5 63 0.029
146
P NRC002 Narcolepsy 62 0.029
147
P HYP117 Hypertriglyceridemia 61 0.029
148
P RCK004 Rickets 61 0.029
149
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.029
150
PLM033 Pulmonary Embolism 60 0.029
151
c ACT073 Acute Leukemia 60 0.029
152
P PRP029 Porphyria 59 0.029
153
FCT006 Factor V Deficiency 57 0.029
154
CHY002 Chylomicron Retention Disease 57 0.029
155
GST033 Gestational Diabetes 57 0.029
156
VRL011 Viral Infectious Disease 55 0.029
157
PTN001 Patent Foramen Ovale 55 0.029
158
P ECL001 Eclampsia 54 0.029
159
SML033 Small Cell Cancer of the Lung, Somatic 54 0.029
160
KRT002 Keratomalacia 52 0.029
161
PRT011 Protein C Deficiency 52 0.029
162
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 0.029
163
HLL004 Hellp Syndrome 50 0.029
164
CHL061 Childhood Leukemia 49 0.029
165
PRT029 Parathyroid Adenoma 48 0.029
166
HYP043 Hyperandrogenism 47 0.029
167
c INT072 Intestinal Pseudo-Obstruction 46 0.029
168
RLP003 Relapsing Fever 45 0.029
169
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.029
170
IND002 Indolent Systemic Mastocytosis 41 0.029
171
FCT008 Factitious Disorder 41 0.029
172
PHC013 Phaeochromocytoma 41 0.029
173
HYD046 Hydatidiform Mole, Recurrent, 1 41 0.029
174
GST010 Gestational Trophoblastic Neoplasm 41 0.029
175
MRS004 Marshall-Smith Syndrome 40 0.029
176
c OVR058 Ovarian Small Cell Carcinoma 36 0.029
177
GRM001 Germ Cell and Embryonal Cancer 36 0.029
178
DYS006 Dysembryoplastic Neuroepithelial Tumor 35 0.029
179
SPN185 Spinal Cord Infarction 34 0.029
180
P XLN007 X-Linked Disease 34 0.029
181
c ACR088 Aicardi-Goutieres Syndrome 3 33 0.029
182
CNC001 Cancerophobia 33 0.029
183
WRT002 Writing Disorder 27 0.029
184
c CRN174 Coronary Heart Disease 2 20 0.029
185
ISD002 Isodicentric Chromosome 15 Syndrome 16 0.029
186
BNJ001 Benjamin Syndrome 9 0.029
187
TRP005 Trophoblastic Neoplasm 36 0.029