Search results for "hypocalcemia"

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

232 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 49 9.793
2
HYP550 Hypomagnesemia 1, Intestinal 27 5.416
3
c HYP564 Hypocalcemia, Autosomal Dominant 2 18 4.169
4
c KNN007 Kenny-Caffey Syndrome, Type 2 26 4.113
5
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 14 3.414
6
BRT041 Bartter Syndrome with Hypocalcemia 7 2.392
7
HYP025 Hyperphosphatemia 36 0.253
8
P HYP024 Hypoparathyroidism 45 0.239
9
P HYP069 Hyperparathyroidism 50 0.156
10
P PSD015 Pseudohypoparathyroidism 42 0.150
11
HYP005 Hypokalemia 39 0.132
12
P RCK004 Rickets 55 0.125
13
c PRM005 Primary Hyperparathyroidism 56 0.118
14
CLC007 Calcium Metabolism Disease 28 0.118
15
P HYP004 Hypercalcemia 52 0.110
16
P GRV001 Graves' Disease 51 0.110
17
HYP017 Hypophosphatemia 39 0.110
18
P HYP599 Hypoparathyroidism, Familial Isolated 38 0.110
19
P OST001 Osteopetrosis 63 0.102
20
P DGR001 Digeorge Syndrome 51 0.102
21
MRC001 Marchiafava Bignami Disease 42 0.102
22
VTM003 Vitamin Metabolic Disorder 18 0.102
23
P CLC005 Celiac Disease 69 0.093
24
P VLC001 Velocardiofacial Syndrome 61 0.093
25
P HYP086 Hypothyroidism 52 0.093
26
NTR005 Nutritional Deficiency Disease 41 0.093
27
P CRD011 Cardiomyopathy 53 0.083
28
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.083
29
PRT030 Parathyroid Gland Disease 35 0.083
30
THY030 Thyroid Gland Disease 35 0.083
31
P FML068 Familial Hypocalciuric Hypercalcemia 31 0.083
32
c DLT002 Dilated Cardiomyopathy 73 0.072
33
CNG034 Congestive Heart Failure 65 0.072
34
P LKM002 Leukemia 61 0.072
35
P PTT014 Pitt-Hopkins Syndrome 55 0.072
36
P THY032 Thyroiditis 48 0.072
37
P SZR006 Seizure Disorder 48 0.072
38
P HYP076 Hyperthyroidism 48 0.072
39
THR013 Thoracic Outlet Syndrome 47 0.072
40
OST011 Osteomalacia 42 0.072
41
P TRC086 Trichohepatoenteric Syndrome 1 42 0.072
42
RCK007 Rickets, Vitamin D-Resistant, Type Iia 40 0.072
43
BSL009 Basal Ganglia Calcification 37 0.072
44
P KNN002 Kenny-Caffey Syndrome 29 0.072
45
PRS063 Paresthesia 20 0.072
46
P MYC007 Myocardial Infarction 76 0.059
47
ANR002 Aniridia 72 0.059
48
P CNG401 Congenital Heart Disease 68 0.059
49
c SPN225 Spondyloarthropathy 1 66 0.059
50
P ANG001 Angelman Syndrome 66 0.059
51
P HRM001 Hermansky-Pudlak Syndrome 62 0.059
52
THY028 Thyroid Cancer 60 0.059
53
c PNC108 Pancreatitis, Hereditary 59 0.059
54
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.059
55
P HPT021 Hepatitis 58 0.059
56
P LYM026 Lymphoblastic Leukemia 57 0.059
57
P MYL007 Myeloma 54 0.059
58
ADN018 Adenoma 54 0.059
59
ACN002 Acanthosis Nigricans 53 0.059
60
P PRT010 Parathyroid Carcinoma 53 0.059
61
HNT002 Hantavirus Pulmonary Syndrome 52 0.059
62
c MTB001 Metabolic Syndrome X 52 0.059
63
c ACT075 Acute Myocardial Infarction 50 0.059
64
BNC003 Bone Cancer 50 0.059
65
KRT002 Keratomalacia 49 0.059
66
P BRT004 Bartter Disease 48 0.059
67
P NPH009 Nephrolithiasis 48 0.059
68
c ART101 Aortic Valve Disease 2 46 0.059
69
P HYP065 Hyperaldosteronism 45 0.059
70
P DRR001 Diarrhea 45 0.059
71
CRD119 Cardiac Arrest 45 0.059
72
URM002 Uremia 44 0.059
73
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 44 0.059
74
BRN106 Burns 43 0.059
75
PRT019 Protein-Losing Enteropathy 40 0.059
76
P PRT029 Parathyroid Adenoma 39 0.059
77
P VTM008 Vitamin D-Dependent Rickets, Type I 39 0.059
78
NPH003 Nephrocalcinosis 39 0.059
79
P INT191 Intestinal Lymphangiectasia 39 0.059
80
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 38 0.059
81
IMP004 Impetigo 34 0.059
82
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.059
83
c PSD067 Pseudohypoparathyroidism Ia 33 0.059
84
HNN001 Hennekam Syndrome 33 0.059
85
c ATS282 Autosomal Recessive Malignant Osteopetrosis 32 0.059
86
THY001 Thyroid Crisis 31 0.059
87
P ATX010 Ataxia Neuropathy Spectrum 31 0.059
88
VSL002 Visual Epilepsy 31 0.059
89
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.059
90
GRC002 Gracile Bone Dysplasia 29 0.059
91
IMP001 Impetigo Herpetiformis 27 0.059
92
c ALP087 Alpha-Heavy Chain Disease 27 0.059
93
c RNG005 Ring Chromosome 10 21 0.059
94
DHL001 Dahlberg Borer Newcomer Syndrome 17 0.059
95
c SCN043 Secondary Intestinal Lymphangiectasia 16 0.059
96
P ALZ034 Alzheimer Disease 98 0.042
97
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.042
98
c MLT019 Multiple Myeloma 77 0.042
99
P OST002 Osteoporosis 75 0.042
100
P OST005 Osteogenesis Imperfecta 70 0.042
101
c HYP595 Hypertension, Essential 68 0.042
102
P PSR002 Psoriasis 64 0.042
103
c HPT001 Hepatitis C 64 0.042
104
P LPR003 Leprosy 63 0.042
105
GTL001 Gitelman Syndrome 63 0.042
106
P HLP001 Holoprosencephaly 62 0.042
107
CHR103 Charge Syndrome 62 0.042
108
ACR007 Acromegaly 61 0.042
109
TYP007 Typhoid Fever 59 0.042
110
PGT001 Paget's Disease of Bone 57 0.042
111
P PNM007 Pneumonia 56 0.042
112
P THL005 Thalassemia 56 0.042
113
IMG001 Image Syndrome 56 0.042
114
DNG002 Dengue Hemorrhagic Fever 55 0.042
115
BRC012 Brucellosis 55 0.042
116
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 55 0.042
117
DRM006 Dermatitis 54 0.042
118
CRT002 Cartilage-Hair Hypoplasia 53 0.042
119
DFC004 Deficiency Anemia 52 0.042
120
MSL001 Measles 52 0.042
121
P MYP004 Myopathy 50 0.042
122
PSD014 Pseudopseudohypoparathyroidism 50 0.042
123
VRL011 Viral Infectious Disease 50 0.042
124
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 50 0.042
125
SPT005 Spotted Fever 49 0.042
126
JHN001 Johanson-Blizzard Syndrome 49 0.042
127
P SHR029 Short Syndrome 49 0.042
128
c ACT073 Acute Leukemia 49 0.042
129
ACT049 Acute Disseminated Encephalomyelitis 49 0.042
130
ATX019 Ataxia with Vitamin E Deficiency 49 0.042
131
GLC003 Glucose Intolerance 49 0.042
132
TXC005 Toxic Shock Syndrome 49 0.042
133
P ESN007 Eosinophilia 48 0.042
134
P CRN108 Cranioectodermal Dysplasia 1 48 0.042
135
PRP030 Purpura 47 0.042
136
ALP008 Alopecia 47 0.042
137
GTR002 Goiter 47 0.042
138
LPR001 Lepromatous Leprosy 47 0.042
139
TTH006 Tooth Disease 47 0.042
140
c HPT003 Hepatitis a 47 0.042
141
INT075 Intracranial Hypertension 46 0.042
142
P FNC004 Fanconi Syndrome 46 0.042
143
RLP002 Relapsing-Remitting Multiple Sclerosis 46 0.042
144
P PLY019 Polyneuropathy 46 0.042
145
THY103 Thyroid Cancer, Monmedullary, 1 46 0.042
146
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.042
147
NWC001 Newcastle Disease 45 0.042
148
PLM010 Pulmonary Edema 45 0.042
149
P INT068 Intestinal Disease 44 0.042
150
MYL020 Myelomeningocele 44 0.042
151
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 44 0.042
152
P HMR012 Hemorrhagic Fever 44 0.042
153
c OPT055 Optic Atrophy Plus Syndrome 43 0.042
154
P OPH004 Ophthalmoplegia 43 0.042
155
c PND001 Pain Disorder 43 0.042
156
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.042
157
GST009 Gastroschisis 43 0.042
158
GST050 Gastrointestinal System Disease 43 0.042
159
P MLT074 Multiple Endocrine Neoplasia 43 0.042
160
PPL002 Papillary Carcinoma 43 0.042
161
NRN001 Neuroendocrine Carcinoma 42 0.042
162
RNL078 Renal Dysplasia 42 0.042
163
CNN003 Conn's Syndrome 41 0.042
164
DFF036 Differentiated Thyroid Carcinoma 40 0.042
165
HYP315 Hyperparathyroidism, Neonatal 39 0.042
166
MNT002 Mental Depression 39 0.042
167
MCR018 Microcytic Anemia 39 0.042
168
RNL011 Renal Osteodystrophy 39 0.042
169
P CHN059 Chondrocalcinosis 38 0.042
170
HND002 Hand, Foot and Mouth Disease 38 0.042
171
HRM002 Hermaphroditism 37 0.042
172
CLC001 Calciphylaxis 37 0.042
173
c OST131 Osteopetrosis, Autosomal Dominant 2 37 0.042
174
OST004 Osteitis Fibrosa 37 0.042
175
END035 Endocrine Gland Cancer 36 0.042
176
STP004 Staphylococcal Toxic Shock Syndrome 36 0.042
177
P INT063 Intellectual Disability 36 0.042
178
MDT001 Mediterranean Spotted Fever 36 0.042
179
SYN036 Syncope 36 0.042
180
P MLT008 Multinodular Goiter 35 0.042
181
MYC033 Myoclonus 35 0.042
182
P HYP265 Hypotonia 35 0.042
183
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 35 0.042
184
P ACT150 Acute Adrenal Insufficiency 34 0.042
185
HRT007 Heart Cancer 34 0.042
186
JJN008 Jejunoileitis 34 0.042
187
STT004 Steatorrhea 33 0.042
188
OST008 Osteosclerotic Myeloma 33 0.042
189
c OST126 Osteopetrosis, Autosomal Recessive 1 33 0.042
190
MDS022 Mediastinitis 33 0.042
191
P HYP057 Hypervitaminosis D 32 0.042
192
INT088 Intrinsic Factor Deficiency 32 0.042
193
LYM116 Lymph Node Disease 31 0.042
194
LYM020 Lymph Node Cancer 31 0.042
195
c ACT053 Acute Thyroiditis 31 0.042
196
ETH004 Euthyroid Sick Syndrome 31 0.042
197
ATS008 Autosomal Dominant Disease 31 0.042
198
TRC020 Tracheitis 30 0.042
199
HYP347 Hypotonia-Cystinuria Syndrome 29 0.042
200
MNR003 Mineral Metabolism Disease 29 0.042
201
c PRM158 Primary Intestinal Lymphangiectasia 29 0.042
202
ORL022 Oral Erosive Lichen 27 0.042
203
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 27 0.042
204
P RNL066 Renal Tubular Acidosis, Distal, Ad 27 0.042
205
P HYP534 Hypomagnesemia 3, Renal 27 0.042
206
PRN039 Paraneoplastic Syndromes 27 0.042
207
VSC018 Visceral Steatosis 26 0.042
208
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 26 0.042
209
c PSD058 Pseudohypoparathyroidism Ic 26 0.042
210
MDS018 Mediastinal Cancer 24 0.042
211
c ATM068 Autoimmune Hypoparathyroidism 23 0.042
212
VSC008 Vascular Hemostatic Disease 22 0.042
213
2P2001 2p21 Microdeletion Syndrome 21 0.042
214
P HRT017 Heart Tumor 21 0.042
215
c BNG076 Benign Exophthalmos Syndrome 21 0.042
216
c PSD035 Pseudohypoparathyroidism Type 2 20 0.042
217
HYP656 Hypoparathyroidism - Deafness - Renal Disease 18 0.042
218
OCL041 Oculomotor Apraxia Cogan Type 17 0.042
219
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 17 0.042
220
FML229 Familial Cutaneous Collagenoma 16 0.042
221
c MYP088 Myopathy, Tubular Aggregate, 2 15 0.042
222
MLL017 Müllerian Derivatives - Lymphangiectasia - Polydactyly 12 0.042
223
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.042
224
P HYP211 Hypomagnesemia Primary 11 0.042
225
P CRN214 Coronary Heart Disease 5 10 0.042
226
CRN156 Craniofacioskeletal Syndrome 10 0.042
227
BNM008 Bone Mineral Density, Low 10 0.042
228
HYP611 Hypoparathyroidism, X-Linked 10 0.042
229
c CRN177 Coronary Heart Disease 7 10 0.042
230
c ADL079 Adult Heart Tumor 7 0.042
231
CSR002 Casr-Related Disorders 5 0.042
232
THY021 Thyroid Malformation 4 0.042