Search results for "hypocalcemia"

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

240 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 55 11.902
2
HYP550 Hypomagnesemia 1, Intestinal 28 6.497
3
c HYP564 Hypocalcemia, Autosomal Dominant 2 25 5.962
4
c KNN007 Kenny-Caffey Syndrome, Type 2 25 4.208
5
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 14 3.585
6
HYP025 Hyperphosphatemia 46 0.253
7
P HYP024 Hypoparathyroidism 52 0.247
8
P HYP069 Hyperparathyroidism 57 0.152
9
P PSD015 Pseudohypoparathyroidism 44 0.146
10
HYP005 Hypokalemia 51 0.128
11
P GRV001 Graves' Disease 61 0.115
12
P RCK004 Rickets 59 0.115
13
HYP017 Hypophosphatemia 42 0.115
14
P PRM237 Primary Hypomagnesemia 29 0.115
15
P OST001 Osteopetrosis 62 0.107
16
MRC001 Marchiafava Bignami Disease 50 0.107
17
VTM003 Vitamin Metabolic Disorder 33 0.107
18
P HYP086 Hypothyroidism 65 0.099
19
P DGR001 Digeorge Syndrome 52 0.099
20
PRT030 Parathyroid Gland Disease 49 0.099
21
P HYP599 Hypoparathyroidism, Familial Isolated 35 0.099
22
P CLC005 Celiac Disease 67 0.091
23
P VLC001 Velocardiofacial Syndrome 62 0.091
24
THY030 Thyroid Gland Disease 51 0.091
25
P CRD011 Cardiomyopathy 67 0.081
26
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.081
27
BHR001 Behr Syndrome 44 0.081
28
PRS063 Paresthesia 36 0.081
29
c DLT002 Dilated Cardiomyopathy 75 0.070
30
P LKM002 Leukemia 70 0.070
31
HYP056 Hypoglycemia 61 0.070
32
P HYP076 Hyperthyroidism 56 0.070
33
P THY032 Thyroiditis 54 0.070
34
MTB004 Metabolic Acidosis 48 0.070
35
NPH003 Nephrocalcinosis 46 0.070
36
BSL009 Basal Ganglia Calcification 43 0.070
37
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 41 0.070
38
c OST131 Osteopetrosis, Autosomal Dominant 2 40 0.070
39
P FML068 Familial Hypocalciuric Hypercalcemia 38 0.070
40
HYP268 Hypercalciuria, Absorptive 37 0.070
41
RCK007 Rickets, Vitamin D-Resistant, Type Iia 37 0.070
42
P LYM124 Lymphangiectasia, Intestinal 25 0.070
43
HYP611 Hypoparathyroidism, X-Linked 21 0.070
44
P MYC007 Myocardial Infarction 79 0.057
45
CNG034 Congestive Heart Failure 71 0.057
46
P HPT021 Hepatitis 70 0.057
47
THY028 Thyroid Cancer 68 0.057
48
P EPL164 Epilepsy 66 0.057
49
P PSR002 Psoriasis 63 0.057
50
CRD119 Cardiac Arrest 63 0.057
51
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.057
52
P PRT010 Parathyroid Carcinoma 62 0.057
53
c ACT075 Acute Myocardial Infarction 60 0.057
54
P LYM026 Lymphoblastic Leukemia 60 0.057
55
PGT001 Paget's Disease of Bone 59 0.057
56
ADN018 Adenoma 59 0.057
57
P SZR006 Seizure Disorder 57 0.057
58
KRT002 Keratomalacia 54 0.057
59
c PSD067 Pseudohypoparathyroidism Ia 52 0.057
60
BRN106 Burns 52 0.057
61
P HYP065 Hyperaldosteronism 51 0.057
62
P DRR001 Diarrhea 51 0.057
63
URM002 Uremia 50 0.057
64
BRD001 Brody Myopathy 49 0.057
65
OST011 Osteomalacia 48 0.057
66
PRT029 Parathyroid Adenoma 47 0.057
67
ACR041 Acromelic Frontonasal Dysostosis 46 0.057
68
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.057
69
LYM116 Lymph Node Disease 44 0.057
70
BRT030 Birth Defects 43 0.057
71
ATS008 Autosomal Dominant Disease 42 0.057
72
IMP004 Impetigo 42 0.057
73
PRT019 Protein-Losing Enteropathy 41 0.057
74
NTR005 Nutritional Deficiency Disease 39 0.057
75
P VTM008 Vitamin D-Dependent Rickets, Type I 36 0.057
76
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.057
77
HYP347 Hypotonia-Cystinuria Syndrome 33 0.057
78
c OST126 Osteopetrosis, Autosomal Recessive 1 33 0.057
79
THY001 Thyroid Crisis 30 0.057
80
c PSD104 Pseudohypoparathyroidism, Type Ii 28 0.057
81
IMP001 Impetigo Herpetiformis 28 0.057
82
P KNN002 Kenny-Caffey Syndrome 27 0.057
83
GRC002 Gracile Bone Dysplasia 27 0.057
84
c ALP087 Alpha-Heavy Chain Disease 23 0.057
85
c RNG005 Ring Chromosome 10 21 0.057
86
BNM008 Bone Mineral Density, Low 19 0.057
87
MLL022 Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly 16 0.057
88
LYM123 Lymphedema-Hypoparathyroidism Syndrome 16 0.057
89
c SCN043 Secondary Intestinal Lymphangiectasia 13 0.057
90
P MLT019 Multiple Myeloma 80 0.041
91
P HRT032 Heart Disease 76 0.041
92
P LPR003 Leprosy 68 0.041
93
P OST005 Osteogenesis Imperfecta 67 0.041
94
P MYP004 Myopathy 67 0.041
95
P PNM007 Pneumonia 66 0.041
96
ACR007 Acromegaly 65 0.041
97
DFC004 Deficiency Anemia 65 0.041
98
BRC012 Brucellosis 65 0.041
99
P OST002 Osteoporosis 64 0.041
100
CHR103 Charge Syndrome 64 0.041
101
P CRB042 Cerebellar Ataxia 64 0.041
102
P SPN301 Spinocerebellar Ataxia 2 63 0.041
103
P HLP001 Holoprosencephaly 62 0.041
104
DNG002 Dengue Hemorrhagic Fever 62 0.041
105
P MCH002 Machado-Joseph Disease 62 0.041
106
c ACT073 Acute Leukemia 62 0.041
107
TTN003 Tetanus 61 0.041
108
P ESN007 Eosinophilia 61 0.041
109
TXC005 Toxic Shock Syndrome 61 0.041
110
P THL005 Thalassemia 61 0.041
111
P INT068 Intestinal Disease 61 0.041
112
TYP007 Typhoid Fever 61 0.041
113
P INF032 Infertility 61 0.041
114
P NPH009 Nephrolithiasis 60 0.041
115
GTL001 Gitelman Syndrome 60 0.041
116
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.041
117
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.041
118
c HPT003 Hepatitis a 59 0.041
119
PRP030 Purpura 59 0.041
120
CRT002 Cartilage-Hair Hypoplasia 58 0.041
121
P EXN002 Exanthem 57 0.041
122
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.041
123
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.041
124
P EPS003 Episodic Ataxia 56 0.041
125
SPT005 Spotted Fever 56 0.041
126
PLM010 Pulmonary Edema 56 0.041
127
c SPN294 Spinocerebellar Ataxia 1 55 0.041
128
c EPS035 Episodic Ataxia, Type 2 55 0.041
129
P MLT074 Multiple Endocrine Neoplasia 55 0.041
130
IMG001 Image Syndrome 55 0.041
131
P HMR012 Hemorrhagic Fever 55 0.041
132
THY103 Thyroid Cancer, Monmedullary, 1 54 0.041
133
P PLY019 Polyneuropathy 54 0.041
134
GTR002 Goiter 54 0.041
135
P INT063 Intellectual Disability 53 0.041
136
P ATX004 Ataxia 53 0.041
137
INT075 Intracranial Hypertension 53 0.041
138
END035 Endocrine Gland Cancer 52 0.041
139
TTH006 Tooth Disease 52 0.041
140
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 52 0.041
141
P PTT014 Pitt-Hopkins Syndrome 51 0.041
142
MSC072 Muscle Cancer 51 0.041
143
c SPN309 Spinocerebellar Ataxia 6 51 0.041
144
c SPN293 Spinocerebellar Ataxia 12 50 0.041
145
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.041
146
MYL020 Myelomeningocele 50 0.041
147
c SPN304 Spinocerebellar Ataxia 8 50 0.041
148
HRT007 Heart Cancer 50 0.041
149
LPR001 Lepromatous Leprosy 49 0.041
150
PPL002 Papillary Carcinoma 49 0.041
151
c SPN291 Spinocerebellar Ataxia 7 49 0.041
152
c ATS308 Autosomal Dominant Cerebellar Ataxia 49 0.041
153
ACT049 Acute Disseminated Encephalomyelitis 49 0.041
154
c INH020 Inherited Metabolic Disorder 49 0.041
155
HND002 Hand, Foot and Mouth Disease 48 0.041
156
c SPN296 Spinocerebellar Ataxia 17 48 0.041
157
DNT016 Dentatorubro-Pallidoluysian Atrophy 48 0.041
158
SYN036 Syncope 47 0.041
159
TRN044 Transposition of the Great Arteries 47 0.041
160
P CRN108 Cranioectodermal Dysplasia 1 47 0.041
161
CRB027 Cerebellar Disease 47 0.041
162
c HRD026 Hereditary Ataxia 47 0.041
163
RNL011 Renal Osteodystrophy 47 0.041
164
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.041
165
EPS004 Episodic Ataxia/myokymia Syndrome 46 0.041
166
JHN001 Johanson-Blizzard Syndrome 46 0.041
167
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 45 0.041
168
OST003 Osteonecrosis 45 0.041
169
RNL078 Renal Dysplasia 45 0.041
170
INT088 Intrinsic Factor Deficiency 45 0.041
171
P ACT150 Acute Adrenal Insufficiency 45 0.041
172
STP004 Staphylococcal Toxic Shock Syndrome 43 0.041
173
GST009 Gastroschisis 43 0.041
174
THL018 Thalassemia Major 42 0.041
175
MCR018 Microcytic Anemia 42 0.041
176
MDS022 Mediastinitis 41 0.041
177
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.041
178
OST004 Osteitis Fibrosa 41 0.041
179
GST071 Gastrointestinal Carcinoma 41 0.041
180
SCH003 Schizophreniform Disorder 41 0.041
181
LYM020 Lymph Node Cancer 41 0.041
182
c SPN100 Spinocerebellar Ataxia 27 41 0.041
183
ATS010 Autosomal Recessive Disease 41 0.041
184
MLT008 Multinodular Goiter 41 0.041
185
CLC001 Calciphylaxis 40 0.041
186
SXD001 Sex Differentiation Disease 40 0.041
187
STT004 Steatorrhea 40 0.041
188
CDS002 Codas Syndrome 40 0.041
189
P HYP265 Hypotonia 39 0.041
190
ATS009 Autosomal Genetic Disease 39 0.041
191
ETH004 Euthyroid Sick Syndrome 38 0.041
192
c CHR579 Chiari Malformation Type Ii 38 0.041
193
OST115 Osteonecrosis of the Jaw 37 0.041
194
JJN008 Jejunoileitis 37 0.041
195
ATM012 Autoimmune Disease of Blood 37 0.041
196
P HYP057 Hypervitaminosis D 37 0.041
197
VSC018 Visceral Steatosis 37 0.041
198
BNS002 Bone Structure Disease 36 0.041
199
MDS018 Mediastinal Cancer 36 0.041
200
c SPN103 Spinocerebellar Ataxia 31 36 0.041
201
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 36 0.041
202
OST008 Osteosclerotic Myeloma 36 0.041
203
P HRT017 Heart Tumor 35 0.041
204
c DGT005 Digital Arthropathy-Brachydactyly, Familial 35 0.041
205
c SPN094 Spinocerebellar Ataxia 18 35 0.041
206
P PST059 Pustular Psoriasis 35 0.041
207
P XLN007 X-Linked Disease 34 0.041
208
VSC008 Vascular Hemostatic Disease 33 0.041
209
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.041
210
PRN039 Paraneoplastic Syndromes 33 0.041
211
c SPN105 Spinocerebellar Ataxia 4 32 0.041
212
TRC020 Tracheitis 32 0.041
213
FTL007 Fetal Hydantoin Syndrome 30 0.041
214
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 30 0.041
215
c ACT053 Acute Thyroiditis 30 0.041
216
P HYP534 Hypomagnesemia 3, Renal 29 0.041
217
c OST134 Osteopetrosis, Autosomal Recessive 6 28 0.041
218
ATM052 Autoimmune Disease 1 28 0.041
219
c OST125 Osteopetrosis, Autosomal Dominant 1 28 0.041
220
c PSD058 Pseudohypoparathyroidism Ic 25 0.041
221
c OST136 Osteopetrosis, Autosomal Recessive 7 25 0.041
222
c ATM068 Autoimmune Hypoparathyroidism 25 0.041
223
P RNL066 Renal Tubular Acidosis, Distal, Ad 24 0.041
224
c OST137 Osteopetrosis, Autosomal Recessive 4 24 0.041
225
c OST120 Osteopetrosis, Autosomal Recessive 5 23 0.041
226
c EPS015 Episodic Ataxia, Type 7 23 0.041
227
c CRN177 Coronary Heart Disease 7 22 0.041
228
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 22 0.041
229
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 21 0.041
230
c MYP088 Myopathy, Tubular Aggregate, 2 19 0.041
231
c ADL079 Adult Heart Tumor 19 0.041
232
ATM053 Autoimmune Disease 2 19 0.041
233
ATM054 Autoimmune Disease 3 18 0.041
234
ACR079 Acrodysostosis with Multiple Hormone Resistance 17 0.041
235
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 16 0.041
236
THY021 Thyroid Malformation 13 0.041
237
CLL041 Collagenoma, Familial Cutaneous 13 0.041
238
CRN156 Craniofacioskeletal Syndrome 12 0.041
239
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 9 0.041
240
CSR002 Casr-Related Disorders 3 0.041