Search results for "hypocalcemia"

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

290 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 43 10.032
2
c HYP564 Hypocalcemia, Autosomal Dominant 2 19 5.795
3
HYP550 Hypomagnesemia 1, Intestinal 23 5.388
4
c KNN007 Kenny-Caffey Syndrome, Type 2 26 4.098
5
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 14 3.334
6
BRT041 Bartter Syndrome with Hypocalcemia 6 2.382
7
CLC007 Calcium Metabolism Disease 32 0.108
8
P HYP599 Hypoparathyroidism, Familial Isolated 38 0.101
9
END072 Endotheliitis 41 0.094
10
MRC001 Marchiafava Bignami Disease 26 0.094
11
VTM003 Vitamin Metabolic Disorder 24 0.094
12
P HYP024 Hypoparathyroidism 45 0.086
13
P BRS047 Breast Cancer 100 0.077
14
P VLC001 Velocardiofacial Syndrome 57 0.077
15
P HYP069 Hyperparathyroidism 54 0.077
16
P HYP086 Hypothyroidism 51 0.077
17
PRT030 Parathyroid Gland Disease 40 0.077
18
THY030 Thyroid Gland Disease 38 0.077
19
TBR010 Tuberculosis 65 0.066
20
c HPT001 Hepatitis C 65 0.066
21
P HPT021 Hepatitis 63 0.066
22
P LKM002 Leukemia 63 0.066
23
P LYM118 Lymphoma 57 0.066
24
c PSD066 Pseudohypoparathyroidism, Type Ib 49 0.066
25
P THY032 Thyroiditis 49 0.066
26
P DGR001 Digeorge Syndrome 49 0.066
27
P CYS018 Cystitis 49 0.066
28
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 43 0.066
29
P CRV039 Cervicitis 41 0.066
30
HYP025 Hyperphosphatemia 38 0.066
31
PRS063 Paresthesia 38 0.066
32
RCK007 Rickets, Vitamin D-Resistant, Type Iia 29 0.066
33
P RNL014 Renal Cell Carcinoma 81 0.054
34
P OST012 Osteoarthritis 72 0.054
35
P NRB001 Neuroblastoma 69 0.054
36
TTR001 Tetralogy of Fallot 66 0.054
37
THY028 Thyroid Cancer 65 0.054
38
P CLC005 Celiac Disease 63 0.054
39
P OST001 Osteopetrosis 61 0.054
40
P MYL006 Myeloid Leukemia 61 0.054
41
PRT036 Peritonitis 59 0.054
42
P CRD011 Cardiomyopathy 59 0.054
43
P RCK004 Rickets 53 0.054
44
PRS047 Prostatitis 53 0.054
45
P BRT004 Bartter Disease 51 0.054
46
URT039 Urticaria 51 0.054
47
HNN001 Hennekam Syndrome 48 0.054
48
BNC003 Bone Cancer 47 0.054
49
P DRR001 Diarrhea 45 0.054
50
GST053 Gastric Cancer 44 0.054
51
TTH006 Tooth Disease 43 0.054
52
KRT002 Keratomalacia 42 0.054
53
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 41 0.054
54
NPH003 Nephrocalcinosis 40 0.054
55
NTR005 Nutritional Deficiency Disease 39 0.054
56
P VTM008 Vitamin D-Dependent Rickets, Type I 36 0.054
57
BSL009 Basal Ganglia Calcification 35 0.054
58
c ATS282 Autosomal Recessive Malignant Osteopetrosis 34 0.054
59
c ACT004 Acute Diarrhea 31 0.054
60
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.054
61
c PSD067 Pseudohypoparathyroidism Ia 30 0.054
62
GRC002 Gracile Bone Dysplasia 28 0.054
63
P KNN002 Kenny-Caffey Syndrome 27 0.054
64
c ALP087 Alpha-Heavy Chain Disease 27 0.054
65
c RNG005 Ring Chromosome 10 21 0.054
66
P HYP211 Hypomagnesemia Primary 16 0.054
67
DHL001 Dahlberg Borer Newcomer Syndrome 16 0.054
68
c SCN043 Secondary Intestinal Lymphangiectasia 14 0.054
69
P CLR023 Colorectal Cancer 91 0.038
70
P PRS040 Prostate Cancer 87 0.038
71
P OBS005 Obesity 87 0.038
72
P RHM011 Rheumatoid Arthritis 87 0.038
73
HPT023 Hepatocellular Carcinoma 87 0.038
74
c SYS001 Systemic Lupus Erythematosus 84 0.038
75
P PLM037 Pulmonary Hypertension 78 0.038
76
P AST005 Asthma 77 0.038
77
MLR004 Malaria 75 0.038
78
c DLT002 Dilated Cardiomyopathy 72 0.038
79
c MLT019 Multiple Myeloma 71 0.038
80
P PHC003 Pheochromocytoma 70 0.038
81
P FLL037 Follicular Lymphoma 70 0.038
82
P OVR042 Ovarian Cancer 69 0.038
83
PTZ001 Peutz-Jeghers Syndrome 68 0.038
84
P OST005 Osteogenesis Imperfecta 67 0.038
85
INS024 Insulin-Like Growth Factor I 67 0.038
86
SCK003 Sickle Cell Anemia 66 0.038
87
c CNG401 Congenital Heart Disease 64 0.038
88
ALL003 Allergic Rhinitis 64 0.038
89
PLM001 Pulmonary Tuberculosis 63 0.038
90
P ART022 Arthritis 63 0.038
91
c HPT073 Hepatitis C Virus 62 0.038
92
ACR007 Acromegaly 62 0.038
93
c MLT136 Multiple Endocrine Neoplasia 1 61 0.038
94
MYC006 Mycosis Fungoides 60 0.038
95
P LPS004 Lupus Erythematosus 59 0.038
96
CHR103 Charge Syndrome 59 0.038
97
P BCL006 B-Cell Lymphomas 59 0.038
98
P ADN016 Adenocarcinoma 59 0.038
99
P CHR071 Charcot-Marie-Tooth Disease 58 0.038
100
P MYS003 Myasthenia Gravis 58 0.038
101
ATP002 Atopy 58 0.038
102
CHG001 Chagas Disease 57 0.038
103
P AST007 Astrocytoma 57 0.038
104
P GLB002 Glioblastoma 56 0.038
105
P PNM007 Pneumonia 56 0.038
106
TTN003 Tetanus 56 0.038
107
ALC006 Alcoholic Hepatitis 56 0.038
108
P GST044 Gastritis 55 0.038
109
P PRT010 Parathyroid Carcinoma 55 0.038
110
P MYP004 Myopathy 54 0.038
111
P THR014 Thrombocytopenia 54 0.038
112
CHR072 Chordoma 53 0.038
113
P GRV001 Graves' Disease 53 0.038
114
P PNC044 Pancreatitis 53 0.038
115
c MTB001 Metabolic Syndrome X 53 0.038
116
P RHN004 Rhinitis 52 0.038
117
P PLC011 Pilocytic Astrocytoma 52 0.038
118
P PTT014 Pitt-Hopkins Syndrome 52 0.038
119
P HRD011 Hereditary Spherocytosis 51 0.038
120
OBS061 Obstructive Sleep Apnea 51 0.038
121
INT066 Interstitial Lung Disease 51 0.038
122
HLY001 Hailey-Hailey Disease 51 0.038
123
P GLM007 Glomerulonephritis 50 0.038
124
LNG099 Lung Disease 50 0.038
125
P LMY004 Leiomyosarcoma 50 0.038
126
THY103 Thyroid Cancer, Monmedullary, 1 50 0.038
127
P ENC004 Encephalitis 50 0.038
128
P MYL007 Myeloma 50 0.038
129
ISC004 Ischemia 49 0.038
130
DFF005 Diffuse Large B-Cell Lymphoma 49 0.038
131
P CRN108 Cranioectodermal Dysplasia 1 49 0.038
132
P HYP098 Hypereosinophilic Syndrome 49 0.038
133
P DDN001 Duodenal Ulcer 49 0.038
134
HDR002 Hidradenitis Suppurativa 48 0.038
135
P MYP006 Myopia 48 0.038
136
BLR001 Biliary Atresia 48 0.038
137
ACS001 Acoustic Neuroma 48 0.038
138
CLN015 Colon Adenocarcinoma 48 0.038
139
JHN001 Johanson-Blizzard Syndrome 48 0.038
140
VRL011 Viral Infectious Disease 48 0.038
141
P NPH009 Nephrolithiasis 48 0.038
142
VGN023 Vaginitis 47 0.038
143
PRT014 Protein S Deficiency 47 0.038
144
P ANG015 Angioedema 47 0.038
145
CHL067 Cholecystitis 47 0.038
146
CYT008 Cytomegalovirus Infection 47 0.038
147
GST033 Gestational Diabetes 47 0.038
148
STL001 St. Louis Encephalitis 47 0.038
149
P HYP065 Hyperaldosteronism 47 0.038
150
ACT049 Acute Disseminated Encephalomyelitis 47 0.038
151
c HPT003 Hepatitis a 47 0.038
152
P NRP001 Neuropathy 47 0.038
153
P SLP006 Sleep Apnea 47 0.038
154
P ACT105 Acute Mountain Sickness 47 0.038
155
CYS014 Cystadenocarcinoma 46 0.038
156
TNS005 Tonsillitis 46 0.038
157
P RTN025 Retinoschisis 46 0.038
158
PLV003 Pelvic Inflammatory Disease 46 0.038
159
LPM004 Lipoma 46 0.038
160
PYG006 Pyogenic Granuloma 46 0.038
161
GST045 Gastroenteritis 46 0.038
162
RTN017 Retinal Detachment 46 0.038
163
MGC001 Megacolon 45 0.038
164
HDC001 Headache 45 0.038
165
HYP080 Hypogonadism 45 0.038
166
PPL002 Papillary Carcinoma 45 0.038
167
CRT049 Critical Limb Ischemia 45 0.038
168
P VSC005 Vesicoureteral Reflux 45 0.038
169
NWC001 Newcastle Disease 45 0.038
170
SPN020 Spondylosis 45 0.038
171
P INT143 Interstitial Cystitis 44 0.038
172
HPR003 Heparin-Induced Thrombocytopenia 44 0.038
173
P PYL005 Pyelonephritis 44 0.038
174
NRM004 Neuroma 44 0.038
175
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 44 0.038
176
IMG001 Image Syndrome 44 0.038
177
MCS003 Mucous Membrane Pemphigoid 44 0.038
178
P STF001 Stiff-Person Syndrome 44 0.038
179
HYP005 Hypokalemia 44 0.038
180
LPD011 Lipoid Adrenal Hyperplasia 44 0.038
181
HND002 Hand, Foot and Mouth Disease 44 0.038
182
CRT002 Cartilage-Hair Hypoplasia 44 0.038
183
VCC001 Vaccinia 43 0.038
184
BLL004 Bullous Keratopathy 43 0.038
185
KRT008 Keratopathy 43 0.038
186
LMB062 Limb Ischemia 43 0.038
187
PRC012 Pericardial Effusion 43 0.038
188
NRN004 Neuroendocrine Tumor 43 0.038
189
P ATR005 Atrophic Gastritis 42 0.038
190
RTN023 Retinitis 42 0.038
191
ACT032 Acute Hemorrhagic Leukoencephalitis 41 0.038
192
END035 Endocrine Gland Cancer 41 0.038
193
FLL008 Folliculitis 41 0.038
194
IGG001 Iga Glomerulonephritis 41 0.038
195
P SCL009 Sclerosing Cholangitis 41 0.038
196
BYS001 Byssinosis 40 0.038
197
TBR008 Tuberculous Peritonitis 40 0.038
198
P GND004 Gonadal Dysgenesis 40 0.038
199
P CHL066 Cholangitis 40 0.038
200
LPM005 Lipomatosis 40 0.038
201
c CHR417 Chronic Graft Versus Host Disease 39 0.038
202
SDD007 Sudden Cardiac Death 39 0.038
203
HDR003 Hidradenitis 39 0.038
204
GYN001 Gynecomastia 39 0.038
205
DDN006 Duodenitis 39 0.038
206
HRT007 Heart Cancer 38 0.038
207
P CTN015 Cutaneous T Cell Lymphoma 38 0.038
208
BRN106 Burns 38 0.038
209
MLT075 Multifocal Motor Neuropathy 38 0.038
210
MSC072 Muscle Cancer 37 0.038
211
P INT191 Intestinal Lymphangiectasia 37 0.038
212
c OST131 Osteopetrosis, Autosomal Dominant 2 37 0.038
213
PRG008 Paragonimiasis 37 0.038
214
BLL003 Bell's Palsy 37 0.038
215
ALL014 Allergic Encephalomyelitis 37 0.038
216
LYM116 Lymph Node Disease 36 0.038
217
URT008 Urticaria Pigmentosa 36 0.038
218
DYS015 Dysentery 36 0.038
219
EST005 Esotropia 36 0.038
220
TXC011 Toxocariasis 35 0.038
221
TTN001 Tetanus Neonatorum 35 0.038
222
RCT011 Rectal Prolapse 35 0.038
223
ATS008 Autosomal Dominant Disease 34 0.038
224
c OST124 Osteogenesis Imperfecta, Type V 34 0.038
225
EVN001 Evans' Syndrome 34 0.038
226
FLT004 Fletcher Factor Deficiency 34 0.038
227
P END039 Endodermal Sinus Tumor 34 0.038
228
XNT001 Xanthogranulomatous Pyelonephritis 34 0.038
229
PRR013 Prurigo Nodularis 34 0.038
230
ERY004 Erysipelas 33 0.038
231
WBR001 Weber Syndrome 33 0.038
232
LYM020 Lymph Node Cancer 33 0.038
233
MNR003 Mineral Metabolism Disease 33 0.038
234
MCN008 Mucinous Cystadenocarcinoma 32 0.038
235
ZYG002 Zygomycosis 32 0.038
236
CLR007 Colorado Tick Fever 32 0.038
237
c OST126 Osteopetrosis, Autosomal Recessive 1 32 0.038
238
MDS022 Mediastinitis 32 0.038
239
CYS003 Cystitis Cystica 32 0.038
240
P FML068 Familial Hypocalciuric Hypercalcemia 32 0.038
241
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 31 0.038
242
GST071 Gastrointestinal Carcinoma 31 0.038
243
ORL022 Oral Erosive Lichen 30 0.038
244
IDP073 Idiopathic Hypercalciuria 30 0.038
245
c PRM158 Primary Intestinal Lymphangiectasia 30 0.038
246
MDS018 Mediastinal Cancer 30 0.038
247
HYP315 Hyperparathyroidism, Neonatal 30 0.038
248
CMP035 Complete Atrioventricular Canal 30 0.038
249
SXD001 Sex Differentiation Disease 30 0.038
250
PLV001 Pelvic Lipomatosis 29 0.038
251
P XLN110 X-Linked Charcot-Marie-Tooth Disease 29 0.038
252
HYP347 Hypotonia-Cystinuria Syndrome 29 0.038
253
VSC018 Visceral Steatosis 29 0.038
254
CNG069 Congenital Cytomegalovirus 28 0.038
255
HMC014 Homocysteinemia 28 0.038
256
EMP002 Emphysematous Cholecystitis 28 0.038
257
c PRM032 Primary Congenital Glaucoma 27 0.038
258
ACC003 Accommodative Esotropia 27 0.038
259
TNS014 Tenosynovitis 27 0.038
260
HRS011 Horseshoe Kidney 27 0.038
261
P RNL066 Renal Tubular Acidosis, Distal, Ad 27 0.038
262
CYT004 Cytomegalic Inclusion Disease 25 0.038
263
c PSD058 Pseudohypoparathyroidism Ic 25 0.038
264
DBT076 Diabetic Embryopathy 25 0.038
265
P HYP534 Hypomagnesemia 3, Renal 24 0.038
266
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 24 0.038
267
BNM005 Bone Marrow Necrosis 24 0.038
268
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 23 0.038
269
VSC008 Vascular Hemostatic Disease 21 0.038
270
BNM008 Bone Mineral Density, Low 21 0.038
271
ELS004 Elastofibroma Dorsi 20 0.038
272
2P2001 2p21 Microdeletion Syndrome 19 0.038
273
FML229 Familial Cutaneous Collagenoma 18 0.038
274
c BNG076 Benign Exophthalmos Syndrome 17 0.038
275
c PSD035 Pseudohypoparathyroidism Type 2 17 0.038
276
P HRT017 Heart Tumor 17 0.038
277
BSL013 Basaloid Follicular Hamartoma 17 0.038
278
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 17 0.038
279
BCP001 Bicipital Tenosynovitis 17 0.038
280
HYP666 Hypoparathyroidism-Deafness-Renal Disease Syndrome 16 0.038
281
c MYP088 Myopathy, Tubular Aggregate, 2 16 0.038
282
c CRN214 Coronary Heart Disease 5 13 0.038
283
c CRN177 Coronary Heart Disease 7 13 0.038
284
MLL020 MĀ³llerian Derivatives-Lymphangiectasia-Polydactyly Syndrome 12 0.038
285
HYP611 Hypoparathyroidism, X-Linked 10 0.038
286
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 10 0.038
287
CRN156 Craniofacioskeletal Syndrome 10 0.038
288
c ADL079 Adult Heart Tumor 9 0.038
289
THY021 Thyroid Malformation 6 0.038
290
CSR002 Casr-Related Disorders 3 0.038