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 56 12.316
2
HYP550 Hypomagnesemia 1, Intestinal 39 8.427
3
c HYP564 Hypocalcemia, Autosomal Dominant 2 24 6.169
4
c KNN007 Kenny-Caffey Syndrome, Type 2 25 4.355
5
HYP025 Hyperphosphatemia 47 0.251
6
P HYP024 Hypoparathyroidism 53 0.244
7
P HYP069 Hyperparathyroidism 58 0.150
8
P PSD015 Pseudohypoparathyroidism 46 0.145
9
HYP005 Hypokalemia 51 0.127
10
P OST001 Osteopetrosis 63 0.114
11
P RCK004 Rickets 61 0.114
12
P GRV001 Graves' Disease 59 0.114
13
HYP017 Hypophosphatemia 43 0.114
14
PRM237 Primary Hypomagnesemia 42 0.114
15
VTM003 Vitamin Metabolic Disorder 30 0.106
16
P HYP086 Hypothyroidism 64 0.098
17
P DGR001 Digeorge Syndrome 53 0.098
18
PRT030 Parathyroid Gland Disease 47 0.098
19
P HYP599 Hypoparathyroidism, Familial Isolated 34 0.098
20
P CLC005 Celiac Disease 68 0.090
21
P VLC001 Velocardiofacial Syndrome 62 0.090
22
c PSD066 Pseudohypoparathyroidism, Type Ib 51 0.090
23
THY030 Thyroid Gland Disease 48 0.090
24
P CRD011 Cardiomyopathy 68 0.080
25
P FML068 Familial Hypocalciuric Hypercalcemia 46 0.080
26
BHR001 Behr Syndrome 42 0.080
27
PRS063 Paresthesia 36 0.080
28
c DLT002 Dilated Cardiomyopathy 76 0.070
29
P LKM002 Leukemia 71 0.070
30
HYP056 Hypoglycemia 61 0.070
31
P HYP076 Hyperthyroidism 55 0.070
32
P THY032 Thyroiditis 54 0.070
33
c PSD067 Pseudohypoparathyroidism Ia 52 0.070
34
MTB004 Metabolic Acidosis 48 0.070
35
NPH003 Nephrocalcinosis 48 0.070
36
BSL009 Basal Ganglia Calcification 43 0.070
37
c OST131 Osteopetrosis, Autosomal Dominant 2 41 0.070
38
RCK007 Rickets, Vitamin D-Resistant, Type Iia 37 0.070
39
HYP268 Hypercalciuria, Absorptive 35 0.070
40
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 34 0.070
41
c PSD104 Pseudohypoparathyroidism, Type Ii 32 0.070
42
P MYC007 Myocardial Infarction 79 0.057
43
CNG034 Congestive Heart Failure 72 0.057
44
THY028 Thyroid Cancer 69 0.057
45
P HPT021 Hepatitis 69 0.057
46
P EPL164 Epilepsy 66 0.057
47
P PRT010 Parathyroid Carcinoma 63 0.057
48
P LYM026 Lymphoblastic Leukemia 62 0.057
49
P PSR002 Psoriasis 61 0.057
50
CRD119 Cardiac Arrest 61 0.057
51
c ACT075 Acute Myocardial Infarction 60 0.057
52
PGT001 Paget's Disease of Bone 59 0.057
53
ADN018 Adenoma 58 0.057
54
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.057
55
P SZR006 Seizure Disorder 56 0.057
56
BRN106 Burns 52 0.057
57
KRT002 Keratomalacia 52 0.057
58
P HYP065 Hyperaldosteronism 50 0.057
59
c KNN009 Kenny-Caffey Syndrome, Type 1 50 0.057
60
OST011 Osteomalacia 49 0.057
61
URM002 Uremia 48 0.057
62
PRT029 Parathyroid Adenoma 48 0.057
63
LYM116 Lymph Node Disease 47 0.057
64
BRD001 Brody Myopathy 47 0.057
65
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.057
66
ACR041 Acromelic Frontonasal Dysostosis 45 0.057
67
BRT030 Birth Defects 43 0.057
68
IMP004 Impetigo 42 0.057
69
HYP347 Hypotonia-Cystinuria Syndrome 42 0.057
70
PRT019 Protein-Losing Enteropathy 42 0.057
71
ATS008 Autosomal Dominant Disease 39 0.057
72
P VTM008 Vitamin D-Dependent Rickets, Type I 36 0.057
73
NTR005 Nutritional Deficiency Disease 36 0.057
74
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.057
75
c OST126 Osteopetrosis, Autosomal Recessive 1 34 0.057
76
c ATM068 Autoimmune Hypoparathyroidism 30 0.057
77
PRM243 Primary Bone Cancer 29 0.057
78
c PSD058 Pseudohypoparathyroidism Ic 28 0.057
79
IMP001 Impetigo Herpetiformis 28 0.057
80
THY001 Thyroid Crisis 27 0.057
81
GRC002 Gracile Bone Dysplasia 24 0.057
82
c ALP087 Alpha-Heavy Chain Disease 23 0.057
83
P LYM124 Lymphangiectasia, Intestinal 21 0.057
84
HYP611 Hypoparathyroidism, X-Linked 20 0.057
85
c RNG005 Ring Chromosome 10 20 0.057
86
ACR079 Acrodysostosis with Multiple Hormone Resistance 19 0.057
87
LYM123 Lymphedema-Hypoparathyroidism Syndrome 16 0.057
88
BNM008 Bone Mineral Density, Low 16 0.057
89
CLC053 Colchicine Poisoning 15 0.057
90
c SCN043 Secondary Intestinal Lymphangiectasia 13 0.057
91
P MLT019 Multiple Myeloma 83 0.040
92
P HRT032 Heart Disease 75 0.040
93
P LPR003 Leprosy 69 0.040
94
P OST005 Osteogenesis Imperfecta 69 0.040
95
P PNM007 Pneumonia 68 0.040
96
P MYP004 Myopathy 67 0.040
97
BRC012 Brucellosis 66 0.040
98
ACR007 Acromegaly 66 0.040
99
P THL005 Thalassemia 64 0.040
100
DFC004 Deficiency Anemia 64 0.040
101
P OST002 Osteoporosis 64 0.040
102
DNG002 Dengue Hemorrhagic Fever 63 0.040
103
P CRB042 Cerebellar Ataxia 63 0.040
104
P HLP001 Holoprosencephaly 63 0.040
105
P MCH002 Machado-Joseph Disease 63 0.040
106
CHR103 Charge Syndrome 62 0.040
107
GTL001 Gitelman Syndrome 61 0.040
108
TYP007 Typhoid Fever 61 0.040
109
TTN003 Tetanus 61 0.040
110
P NPH009 Nephrolithiasis 60 0.040
111
P INT068 Intestinal Disease 60 0.040
112
TXC005 Toxic Shock Syndrome 60 0.040
113
c ACT073 Acute Leukemia 60 0.040
114
P DRR001 Diarrhea 60 0.040
115
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.040
116
c HPT003 Hepatitis a 59 0.040
117
P INF032 Infertility 59 0.040
118
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.040
119
PRP030 Purpura 58 0.040
120
P EXN002 Exanthem 57 0.040
121
CRT002 Cartilage-Hair Hypoplasia 57 0.040
122
P EPS003 Episodic Ataxia 57 0.040
123
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.040
124
P MLT074 Multiple Endocrine Neoplasia 56 0.040
125
P PLY019 Polyneuropathy 56 0.040
126
P SPN301 Spinocerebellar Ataxia 2 56 0.040
127
P HMR012 Hemorrhagic Fever 56 0.040
128
c SPN294 Spinocerebellar Ataxia 1 55 0.040
129
PLM010 Pulmonary Edema 54 0.040
130
RST001 Restless Legs Syndrome 54 0.040
131
THY103 Thyroid Cancer, Monmedullary, 1 53 0.040
132
SPT005 Spotted Fever 53 0.040
133
GTR002 Goiter 52 0.040
134
TTH006 Tooth Disease 52 0.040
135
c SPN291 Spinocerebellar Ataxia 7 51 0.040
136
PPL002 Papillary Carcinoma 51 0.040
137
c EPS035 Episodic Ataxia, Type 2 51 0.040
138
c SPN309 Spinocerebellar Ataxia 6 51 0.040
139
MYL020 Myelomeningocele 51 0.040
140
c SPN293 Spinocerebellar Ataxia 12 50 0.040
141
IMG001 Image Syndrome 50 0.040
142
LPR001 Lepromatous Leprosy 50 0.040
143
INT075 Intracranial Hypertension 50 0.040
144
END035 Endocrine Gland Cancer 49 0.040
145
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.040
146
MSC072 Muscle Cancer 49 0.040
147
P INT063 Intellectual Disability 49 0.040
148
c INH020 Inherited Metabolic Disorder 49 0.040
149
P FNC004 Fanconi Syndrome 49 0.040
150
CCN001 Cocaine Dependence 49 0.040
151
TRN044 Transposition of the Great Arteries 48 0.040
152
c ATS308 Autosomal Dominant Cerebellar Ataxia 48 0.040
153
THL018 Thalassemia Major 48 0.040
154
c SPN296 Spinocerebellar Ataxia 17 48 0.040
155
P CRN108 Cranioectodermal Dysplasia 1 48 0.040
156
DNT016 Dentatorubro-Pallidoluysian Atrophy 47 0.040
157
P PTT014 Pitt-Hopkins Syndrome 47 0.040
158
CRB027 Cerebellar Disease 47 0.040
159
HND002 Hand, Foot and Mouth Disease 47 0.040
160
GST009 Gastroschisis 47 0.040
161
SYN036 Syncope 47 0.040
162
HRT007 Heart Cancer 46 0.040
163
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.040
164
CLC001 Calciphylaxis 46 0.040
165
JHN001 Johanson-Blizzard Syndrome 46 0.040
166
P ACT150 Acute Adrenal Insufficiency 45 0.040
167
RNL078 Renal Dysplasia 45 0.040
168
EPS004 Episodic Ataxia/myokymia Syndrome 45 0.040
169
OST003 Osteonecrosis 45 0.040
170
INT088 Intrinsic Factor Deficiency 45 0.040
171
RNL011 Renal Osteodystrophy 45 0.040
172
c HRD026 Hereditary Ataxia 44 0.040
173
MCR018 Microcytic Anemia 43 0.040
174
c SPN100 Spinocerebellar Ataxia 27 43 0.040
175
GST071 Gastrointestinal Carcinoma 42 0.040
176
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.040
177
P CHN059 Chondrocalcinosis 41 0.040
178
STP004 Staphylococcal Toxic Shock Syndrome 41 0.040
179
ATS010 Autosomal Recessive Disease 41 0.040
180
MLT008 Multinodular Goiter 41 0.040
181
OST004 Osteitis Fibrosa 41 0.040
182
MDS022 Mediastinitis 41 0.040
183
P KNN002 Kenny-Caffey Syndrome 41 0.040
184
STT004 Steatorrhea 40 0.040
185
SCH003 Schizophreniform Disorder 40 0.040
186
CMB023 Combined Immunodeficiency, X-Linked, Moderate 40 0.040
187
HRN003 Heroin Dependence 40 0.040
188
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.040
189
LYM020 Lymph Node Cancer 39 0.040
190
P HYP265 Hypotonia 38 0.040
191
c HYP314 Hypocalciuric Hypercalcemia, Type I 38 0.040
192
JJN008 Jejunoileitis 38 0.040
193
c SPN103 Spinocerebellar Ataxia 31 38 0.040
194
SXD001 Sex Differentiation Disease 38 0.040
195
OST115 Osteonecrosis of the Jaw 38 0.040
196
P HYP057 Hypervitaminosis D 38 0.040
197
CDS002 Codas Syndrome 37 0.040
198
c CHR579 Chiari Malformation Type Ii 37 0.040
199
VSC018 Visceral Steatosis 37 0.040
200
BNS002 Bone Structure Disease 37 0.040
201
P PST059 Pustular Psoriasis 36 0.040
202
c HYP317 Hypocalciuric Hypercalcemia, Type Ii 36 0.040
203
ETH004 Euthyroid Sick Syndrome 36 0.040
204
MDS018 Mediastinal Cancer 36 0.040
205
OST008 Osteosclerotic Myeloma 36 0.040
206
c SPN094 Spinocerebellar Ataxia 18 35 0.040
207
ATM012 Autoimmune Disease of Blood 35 0.040
208
ATS009 Autosomal Genetic Disease 35 0.040
209
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 34 0.040
210
c OST129 Osteopetrosis, Autosomal Recessive 2 34 0.040
211
P XLN007 X-Linked Disease 34 0.040
212
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 33 0.040
213
c DGT005 Digital Arthropathy-Brachydactyly, Familial 33 0.040
214
P HRT017 Heart Tumor 32 0.040
215
FTL007 Fetal Hydantoin Syndrome 32 0.040
216
PRN039 Paraneoplastic Syndromes 32 0.040
217
TRC020 Tracheitis 31 0.040
218
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 31 0.040
219
VSC008 Vascular Hemostatic Disease 30 0.040
220
c ACT053 Acute Thyroiditis 30 0.040
221
P HYP534 Hypomagnesemia 3, Renal 29 0.040
222
c OST125 Osteopetrosis, Autosomal Dominant 1 29 0.040
223
c OST134 Osteopetrosis, Autosomal Recessive 6 28 0.040
224
c OST136 Osteopetrosis, Autosomal Recessive 7 26 0.040
225
ATM052 Autoimmune Disease 1 25 0.040
226
P RNL066 Renal Tubular Acidosis, Distal, Ad 24 0.040
227
c OST137 Osteopetrosis, Autosomal Recessive 4 24 0.040
228
c OST120 Osteopetrosis, Autosomal Recessive 5 24 0.040
229
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 24 0.040
230
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 23 0.040
231
c EPS015 Episodic Ataxia, Type 7 23 0.040
232
c PRM158 Primary Intestinal Lymphangiectasia 23 0.040
233
c CRN214 Coronary Heart Disease 5 22 0.040
234
c CRN177 Coronary Heart Disease 7 20 0.040
235
c MYP088 Myopathy, Tubular Aggregate, 2 20 0.040
236
c BRT048 Bartter Disease Type 5 17 0.040
237
c ADL079 Adult Heart Tumor 16 0.040
238
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 16 0.040
239
MLL022 Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly 16 0.040
240
ATM053 Autoimmune Disease 2 16 0.040
241
ATM054 Autoimmune Disease 3 15 0.040
242
CRN156 Craniofacioskeletal Syndrome 12 0.040
243
THY021 Thyroid Malformation 11 0.040
244
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 9 0.040
245
CSR002 Casr-Related Disorders 3 0.040