Search results for "hypocalcemia"

The MalaCard for "hypocalcemia" has been retired.
Searching MalaCards for entries containing "hypocalcemia"

245 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 50 11.161
2
HYP550 Hypomagnesemia 1, Intestinal 28 6.505
3
c HYP564 Hypocalcemia, Autosomal Dominant 2 22 5.971
4
c KNN007 Kenny-Caffey Syndrome, Type 2 26 4.208
5
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 17 3.603
6
HYP025 Hyperphosphatemia 45 0.251
7
P HYP024 Hypoparathyroidism 52 0.242
8
P HYP069 Hyperparathyroidism 57 0.156
9
HYP005 Hypokalemia 52 0.134
10
P PSD015 Pseudohypoparathyroidism 43 0.134
11
CLC007 Calcium Metabolism Disease 39 0.127
12
P PRM237 Primary Hypomagnesemia 28 0.121
13
P RCK004 Rickets 59 0.114
14
c PRM005 Primary Hyperparathyroidism 56 0.114
15
P OST001 Osteopetrosis 63 0.114
16
HYP017 Hypophosphatemia 43 0.114
17
P HYP599 Hypoparathyroidism, Familial Isolated 35 0.106
18
P GRV001 Graves' Disease 62 0.106
19
MRC001 Marchiafava Bignami Disease 33 0.106
20
VTM003 Vitamin Metabolic Disorder 31 0.106
21
P DGR001 Digeorge Syndrome 52 0.099
22
P HYP086 Hypothyroidism 63 0.099
23
PRT030 Parathyroid Gland Disease 49 0.099
24
P HYP004 Hypercalcemia 54 0.099
25
PRS063 Paresthesia 30 0.099
26
P VLC001 Velocardiofacial Syndrome 64 0.090
27
P CLC005 Celiac Disease 67 0.090
28
BSL009 Basal Ganglia Calcification 41 0.090
29
HYP268 Hypercalciuria, Absorptive 31 0.090
30
THY030 Thyroid Gland Disease 52 0.090
31
NPH003 Nephrocalcinosis 47 0.090
32
c PSD066 Pseudohypoparathyroidism, Type Ib 49 0.081
33
BHR001 Behr Syndrome 43 0.081
34
P CRD011 Cardiomyopathy 66 0.081
35
c DLT002 Dilated Cardiomyopathy 75 0.070
36
c OST131 Osteopetrosis, Autosomal Dominant 2 40 0.070
37
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 42 0.070
38
P LKM002 Leukemia 70 0.070
39
HYP056 Hypoglycemia 60 0.070
40
P HYP076 Hyperthyroidism 59 0.070
41
DBT001 Diabetic Ketoacidosis 45 0.070
42
P FML068 Familial Hypocalciuric Hypercalcemia 37 0.070
43
RCK007 Rickets, Vitamin D-Resistant, Type Iia 26 0.070
44
P HYP065 Hyperaldosteronism 52 0.070
45
P LYM124 Lymphangiectasia, Intestinal 23 0.070
46
P DRR001 Diarrhea 60 0.070
47
P THY032 Thyroiditis 57 0.070
48
MTB004 Metabolic Acidosis 49 0.070
49
P MYC007 Myocardial Infarction 80 0.057
50
P SPN301 Spinocerebellar Ataxia 2 57 0.057
51
P MCH002 Machado-Joseph Disease 63 0.057
52
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.057
53
c SPN294 Spinocerebellar Ataxia 1 54 0.057
54
DNT016 Dentatorubro-Pallidoluysian Atrophy 49 0.057
55
THY028 Thyroid Cancer 71 0.057
56
c EPS035 Episodic Ataxia, Type 2 54 0.057
57
CNG034 Congestive Heart Failure 72 0.057
58
P PTT014 Pitt-Hopkins Syndrome 51 0.057
59
P SZR006 Seizure Disorder 56 0.057
60
P EPS003 Episodic Ataxia 58 0.057
61
KRT002 Keratomalacia 50 0.057
62
EPS004 Episodic Ataxia/myokymia Syndrome 47 0.057
63
CRD119 Cardiac Arrest 63 0.057
64
P PRT010 Parathyroid Carcinoma 61 0.057
65
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.057
66
c SPN309 Spinocerebellar Ataxia 6 48 0.057
67
P HPT021 Hepatitis 74 0.057
68
P PSR002 Psoriasis 63 0.057
69
c ATS308 Autosomal Dominant Cerebellar Ataxia 51 0.057
70
c SPN100 Spinocerebellar Ataxia 27 41 0.057
71
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 45 0.057
72
NTR005 Nutritional Deficiency Disease 51 0.057
73
BRD001 Brody Myopathy 49 0.057
74
GRC002 Gracile Bone Dysplasia 27 0.057
75
P BRT004 Bartter Disease 46 0.057
76
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 34 0.057
77
c PSD067 Pseudohypoparathyroidism Ia 36 0.057
78
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.057
79
c SPN293 Spinocerebellar Ataxia 12 46 0.057
80
c SPN094 Spinocerebellar Ataxia 18 34 0.057
81
c SPN103 Spinocerebellar Ataxia 31 36 0.057
82
P CRB042 Cerebellar Ataxia 64 0.057
83
c SPN105 Spinocerebellar Ataxia 4 32 0.057
84
c HRD026 Hereditary Ataxia 46 0.057
85
ACT049 Acute Disseminated Encephalomyelitis 50 0.057
86
HYP347 Hypotonia-Cystinuria Syndrome 32 0.057
87
P LYM026 Lymphoblastic Leukemia 60 0.057
88
P VTM008 Vitamin D-Dependent Rickets, Type I 36 0.057
89
CYN002 Cyanosis, Transient Neonatal 29 0.057
90
c PSD104 Pseudohypoparathyroidism, Type Ii 27 0.057
91
IMP004 Impetigo 41 0.057
92
MLL022 Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly 17 0.057
93
CRB027 Cerebellar Disease 46 0.057
94
PRT029 Parathyroid Adenoma 46 0.057
95
ADN018 Adenoma 59 0.057
96
P EPL164 Epilepsy 60 0.057
97
c RNG005 Ring Chromosome 10 20 0.057
98
P TRM003 Tremor 54 0.057
99
OST011 Osteomalacia 48 0.057
100
THY001 Thyroid Crisis 29 0.057
101
URM002 Uremia 36 0.057
102
HYP611 Hypoparathyroidism, X-Linked 21 0.057
103
LYM123 Lymphedema-Hypoparathyroidism Syndrome 16 0.057
104
P ATX004 Ataxia 53 0.057
105
c EPS015 Episodic Ataxia, Type 7 22 0.057
106
P MYL007 Myeloma 52 0.057
107
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 22 0.057
108
c ACT075 Acute Myocardial Infarction 61 0.057
109
IMP001 Impetigo Herpetiformis 29 0.057
110
PRT019 Protein-Losing Enteropathy 42 0.057
111
P KNN002 Kenny-Caffey Syndrome 28 0.057
112
c ALP087 Alpha-Heavy Chain Disease 23 0.057
113
BNM008 Bone Mineral Density, Low 28 0.057
114
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.057
115
LYM116 Lymph Node Disease 42 0.057
116
ATS008 Autosomal Dominant Disease 41 0.057
117
BRN106 Burns 52 0.057
118
c SCN043 Secondary Intestinal Lymphangiectasia 14 0.057
119
CSR002 Casr-Related Disorders 3 0.057
120
c MLT019 Multiple Myeloma 77 0.040
121
P OST002 Osteoporosis 63 0.040
122
P OST005 Osteogenesis Imperfecta 68 0.040
123
IMG001 Image Syndrome 54 0.040
124
P AGM005 Agammaglobulinemia, X-Linked 1 60 0.040
125
PGT001 Paget's Disease of Bone 60 0.040
126
GTL001 Gitelman Syndrome 60 0.040
127
P LPR003 Leprosy 70 0.040
128
CHR103 Charge Syndrome 64 0.040
129
ACR007 Acromegaly 66 0.040
130
DFC004 Deficiency Anemia 64 0.040
131
P CRN108 Cranioectodermal Dysplasia 1 48 0.040
132
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 31 0.040
133
THY103 Thyroid Cancer, Monmedullary, 1 55 0.040
134
GMM002 Gamma Chain Deficiency 53 0.040
135
P RNL066 Renal Tubular Acidosis, Distal, Ad 29 0.040
136
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.040
137
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.040
138
CRT002 Cartilage-Hair Hypoplasia 57 0.040
139
ACR041 Acromelic Frontonasal Dysostosis 45 0.040
140
c CNG401 Congenital Heart Disease 67 0.040
141
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 40 0.040
142
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.040
143
JHN001 Johanson-Blizzard Syndrome 47 0.040
144
P INF032 Infertility 61 0.040
145
c OST125 Osteopetrosis, Autosomal Dominant 1 26 0.040
146
P MYP004 Myopathy 67 0.040
147
c PSD058 Pseudohypoparathyroidism Ic 26 0.040
148
TTN003 Tetanus 62 0.040
149
BRC012 Brucellosis 66 0.040
150
INT088 Intrinsic Factor Deficiency 37 0.040
151
c OST136 Osteopetrosis, Autosomal Recessive 7 26 0.040
152
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.040
153
c CHR579 Chiari Malformation Type Ii 38 0.040
154
c OST120 Osteopetrosis, Autosomal Recessive 5 26 0.040
155
c OST137 Osteopetrosis, Autosomal Recessive 4 24 0.040
156
P HLP001 Holoprosencephaly 62 0.040
157
c OST134 Osteopetrosis, Autosomal Recessive 6 29 0.040
158
GTR002 Goiter 54 0.040
159
P THL005 Thalassemia 61 0.040
160
HNN001 Hennekam Syndrome 48 0.040
161
HRT007 Heart Cancer 51 0.040
162
CDS002 Codas Syndrome 38 0.040
163
TYP007 Typhoid Fever 61 0.040
164
c DGT005 Digital Arthropathy-Brachydactyly, Familial 36 0.040
165
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 39 0.040
166
P ESN007 Eosinophilia 61 0.040
167
PRP030 Purpura 60 0.040
168
P PNM007 Pneumonia 67 0.040
169
c HPT003 Hepatitis a 55 0.040
170
SPT005 Spotted Fever 56 0.040
171
P HYP534 Hypomagnesemia 3, Renal 28 0.040
172
P NPH009 Nephrolithiasis 59 0.040
173
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 24 0.040
174
TTH006 Tooth Disease 52 0.040
175
TXC005 Toxic Shock Syndrome 61 0.040
176
ATX003 Ataxia with Isolated Vitamin E Deficiency 36 0.040
177
SVR066 Severe Combined Immunodeficiency, X-Linked 43 0.040
178
CMB023 Combined Immunodeficiency, X-Linked, Moderate 27 0.040
179
c ACT073 Acute Leukemia 61 0.040
180
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 16 0.040
181
P INT068 Intestinal Disease 60 0.040
182
P PLY019 Polyneuropathy 53 0.040
183
PLM010 Pulmonary Edema 56 0.040
184
P FNC004 Fanconi Syndrome 54 0.040
185
P INT063 Intellectual Disability 46 0.040
186
INT075 Intracranial Hypertension 52 0.040
187
MYL020 Myelomeningocele 50 0.040
188
END035 Endocrine Gland Cancer 50 0.040
189
P HMR012 Hemorrhagic Fever 55 0.040
190
ATM052 Autoimmune Disease 1 26 0.040
191
TRN044 Transposition of the Great Arteries 48 0.040
192
LPR001 Lepromatous Leprosy 50 0.040
193
c MYP088 Myopathy, Tubular Aggregate, 2 16 0.040
194
HND002 Hand, Foot and Mouth Disease 49 0.040
195
DNG002 Dengue Hemorrhagic Fever 60 0.040
196
P MLT074 Multiple Endocrine Neoplasia 55 0.040
197
FTL007 Fetal Hydantoin Syndrome 28 0.040
198
RNL078 Renal Dysplasia 48 0.040
199
RNL011 Renal Osteodystrophy 48 0.040
200
c CRN214 Coronary Heart Disease 5 22 0.040
201
STP004 Staphylococcal Toxic Shock Syndrome 43 0.040
202
TRC020 Tracheitis 30 0.040
203
MSC072 Muscle Cancer 47 0.040
204
MCR018 Microcytic Anemia 41 0.040
205
c CRN177 Coronary Heart Disease 7 21 0.040
206
LYM020 Lymph Node Cancer 41 0.040
207
MDS018 Mediastinal Cancer 34 0.040
208
OST004 Osteitis Fibrosa 44 0.040
209
BRT030 Birth Defects 44 0.040
210
c INH020 Inherited Metabolic Disorder 49 0.040
211
CLC001 Calciphylaxis 40 0.040
212
VSC018 Visceral Steatosis 37 0.040
213
ETH004 Euthyroid Sick Syndrome 37 0.040
214
P EXN002 Exanthem 57 0.040
215
CLL041 Collagenoma, Familial Cutaneous 13 0.040
216
STT004 Steatorrhea 41 0.040
217
P ACT150 Acute Adrenal Insufficiency 36 0.040
218
GST009 Gastroschisis 31 0.040
219
P HRT017 Heart Tumor 34 0.040
220
CRN156 Craniofacioskeletal Syndrome 12 0.040
221
MDS022 Mediastinitis 37 0.040
222
JJN008 Jejunoileitis 38 0.040
223
PPL002 Papillary Carcinoma 50 0.040
224
GST071 Gastrointestinal Carcinoma 37 0.040
225
SXD001 Sex Differentiation Disease 39 0.040
226
c ACT053 Acute Thyroiditis 29 0.040
227
MLT008 Multinodular Goiter 40 0.040
228
ATM053 Autoimmune Disease 2 16 0.040
229
ATM054 Autoimmune Disease 3 16 0.040
230
SYN036 Syncope 45 0.040
231
VSC008 Vascular Hemostatic Disease 30 0.040
232
P HYP057 Hypervitaminosis D 36 0.040
233
PRN039 Paraneoplastic Syndromes 42 0.040
234
c ADL079 Adult Heart Tumor 17 0.040
235
ATS009 Autosomal Genetic Disease 38 0.040
236
P PST059 Pustular Psoriasis 33 0.040
237
c ATM068 Autoimmune Hypoparathyroidism 24 0.040
238
THY021 Thyroid Malformation 12 0.040
239
ATM012 Autoimmune Disease of Blood 36 0.040
240
ATS010 Autosomal Recessive Disease 40 0.040
241
ACR079 Acrodysostosis with Multiple Hormone Resistance 18 0.040
242
OST008 Osteosclerotic Myeloma 37 0.040
243
P HYP265 Hypotonia 39 0.040
244
THL018 Thalassemia Major 31 0.040
245
P XLN007 X-Linked Disease 34 0.040