Search results for "hypocalcemia"

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

200 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 46 10.103
2
c HYP564 Hypocalcemia, Autosomal Dominant 2 20 5.837
3
HYP550 Hypomagnesemia 1, Intestinal 27 5.440
4
c KNN007 Kenny-Caffey Syndrome, Type 2 25 4.127
5
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 17 3.429
6
BRT041 Bartter Syndrome with Hypocalcemia 9 2.401
7
HYP025 Hyperphosphatemia 46 0.271
8
P HYP024 Hypoparathyroidism 51 0.249
9
P HYP069 Hyperparathyroidism 57 0.186
10
P PSD015 Pseudohypoparathyroidism 49 0.146
11
HYP005 Hypokalemia 53 0.139
12
P OST001 Osteopetrosis 69 0.124
13
P RCK004 Rickets 62 0.124
14
c PRM005 Primary Hyperparathyroidism 57 0.124
15
HYP017 Hypophosphatemia 43 0.124
16
CLC007 Calcium Metabolism Disease 43 0.124
17
P GRV001 Graves' Disease 65 0.116
18
P HYP599 Hypoparathyroidism, Familial Isolated 34 0.116
19
MRC001 Marchiafava Bignami Disease 54 0.108
20
P HYP004 Hypercalcemia 54 0.108
21
P DGR001 Digeorge Syndrome 53 0.108
22
VTM003 Vitamin Metabolic Disorder 34 0.108
23
P CLC005 Celiac Disease 70 0.098
24
P HYP086 Hypothyroidism 65 0.098
25
P VLC001 Velocardiofacial Syndrome 64 0.098
26
P CRD011 Cardiomyopathy 68 0.088
27
THY030 Thyroid Gland Disease 51 0.088
28
PRT030 Parathyroid Gland Disease 50 0.088
29
c PSD066 Pseudohypoparathyroidism, Type Ib 48 0.088
30
P FML068 Familial Hypocalciuric Hypercalcemia 33 0.088
31
c DLT002 Dilated Cardiomyopathy 74 0.076
32
P LKM002 Leukemia 70 0.076
33
P HYP076 Hyperthyroidism 56 0.076
34
P THY032 Thyroiditis 54 0.076
35
PRS063 Paresthesia 47 0.076
36
BSL009 Basal Ganglia Calcification 44 0.076
37
RCK007 Rickets, Vitamin D-Resistant, Type Iia 42 0.076
38
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 42 0.076
39
P KNN002 Kenny-Caffey Syndrome 28 0.076
40
P MYC007 Myocardial Infarction 80 0.062
41
P HPT021 Hepatitis 77 0.062
42
CNG034 Congestive Heart Failure 72 0.062
43
THY028 Thyroid Cancer 70 0.062
44
P PSR002 Psoriasis 65 0.062
45
c ACT075 Acute Myocardial Infarction 64 0.062
46
P LYM026 Lymphoblastic Leukemia 63 0.062
47
BNC003 Bone Cancer 62 0.062
48
CRD119 Cardiac Arrest 62 0.062
49
ADN018 Adenoma 62 0.062
50
P PRT010 Parathyroid Carcinoma 59 0.062
51
KRT002 Keratomalacia 58 0.062
52
P MYL007 Myeloma 58 0.062
53
P DRR001 Diarrhea 56 0.062
54
NTR005 Nutritional Deficiency Disease 54 0.062
55
P HYP065 Hyperaldosteronism 53 0.062
56
URM002 Uremia 52 0.062
57
OST011 Osteomalacia 50 0.062
58
P BRT004 Bartter Disease 49 0.062
59
HNN001 Hennekam Syndrome 49 0.062
60
P PRT029 Parathyroid Adenoma 48 0.062
61
BRN106 Burns 48 0.062
62
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 47 0.062
63
NPH003 Nephrocalcinosis 47 0.062
64
IMP004 Impetigo 45 0.062
65
PRT019 Protein-Losing Enteropathy 44 0.062
66
P INT191 Intestinal Lymphangiectasia 39 0.062
67
c ATS282 Autosomal Recessive Malignant Osteopetrosis 38 0.062
68
P VTM008 Vitamin D-Dependent Rickets, Type I 38 0.062
69
THY001 Thyroid Crisis 38 0.062
70
c PSD067 Pseudohypoparathyroidism Ia 31 0.062
71
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.062
72
GRC002 Gracile Bone Dysplasia 28 0.062
73
c ALP087 Alpha-Heavy Chain Disease 27 0.062
74
IMP001 Impetigo Herpetiformis 26 0.062
75
P HYP211 Hypomagnesemia Primary 24 0.062
76
c RNG005 Ring Chromosome 10 21 0.062
77
DHL001 Dahlberg Borer Newcomer Syndrome 17 0.062
78
c SCN043 Secondary Intestinal Lymphangiectasia 16 0.062
79
P OST002 Osteoporosis 80 0.044
80
c MLT019 Multiple Myeloma 77 0.044
81
c HPT001 Hepatitis C 72 0.044
82
P LPR003 Leprosy 71 0.044
83
BRC012 Brucellosis 70 0.044
84
c CNG401 Congenital Heart Disease 70 0.044
85
c MLT136 Multiple Endocrine Neoplasia 1 68 0.044
86
P OST005 Osteogenesis Imperfecta 68 0.044
87
P PNM007 Pneumonia 68 0.044
88
DNG002 Dengue Hemorrhagic Fever 67 0.044
89
ACR007 Acromegaly 66 0.044
90
P MYP004 Myopathy 66 0.044
91
TXC005 Toxic Shock Syndrome 66 0.044
92
TYP007 Typhoid Fever 65 0.044
93
P ESN007 Eosinophilia 64 0.044
94
P INT068 Intestinal Disease 64 0.044
95
PGT001 Paget's Disease of Bone 64 0.044
96
c MTB001 Metabolic Syndrome X 64 0.044
97
P HLP001 Holoprosencephaly 63 0.044
98
VRL011 Viral Infectious Disease 62 0.044
99
CHR103 Charge Syndrome 62 0.044
100
GTL001 Gitelman Syndrome 62 0.044
101
P THL005 Thalassemia 62 0.044
102
SPT005 Spotted Fever 61 0.044
103
DFC004 Deficiency Anemia 62 0.044
104
c ACT073 Acute Leukemia 60 0.044
105
HYP056 Hypoglycemia 60 0.044
106
P HMR012 Hemorrhagic Fever 60 0.044
107
c HPT003 Hepatitis a 59 0.044
108
PRP030 Purpura 58 0.044
109
PLM010 Pulmonary Edema 56 0.044
110
GTR002 Goiter 56 0.044
111
P PLY019 Polyneuropathy 55 0.044
112
INT075 Intracranial Hypertension 55 0.044
113
P MLT074 Multiple Endocrine Neoplasia 55 0.044
114
LPR001 Lepromatous Leprosy 55 0.044
115
TTH006 Tooth Disease 54 0.044
116
THY103 Thyroid Cancer, Monmedullary, 1 54 0.044
117
END035 Endocrine Gland Cancer 54 0.044
118
NWC001 Newcastle Disease 54 0.044
119
IMG001 Image Syndrome 53 0.044
120
P FNC004 Fanconi Syndrome 53 0.044
121
DBT001 Diabetic Ketoacidosis 53 0.044
122
ACT049 Acute Disseminated Encephalomyelitis 52 0.044
123
HND002 Hand, Foot and Mouth Disease 52 0.044
124
PPL002 Papillary Carcinoma 52 0.044
125
HRT007 Heart Cancer 52 0.044
126
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 51 0.044
127
P OPH004 Ophthalmoplegia 51 0.044
128
MYL020 Myelomeningocele 51 0.044
129
BND016 Bone Diseases 51 0.044
130
GST009 Gastroschisis 51 0.044
131
MSC072 Muscle Cancer 50 0.044
132
P PTT014 Pitt-Hopkins Syndrome 50 0.044
133
RNL011 Renal Osteodystrophy 49 0.044
134
MTB004 Metabolic Acidosis 49 0.044
135
P CRN108 Cranioectodermal Dysplasia 1 49 0.044
136
P SZR006 Seizure Disorder 48 0.044
137
JHN001 Johanson-Blizzard Syndrome 47 0.044
138
LYM116 Lymph Node Disease 47 0.044
139
P PST059 Pustular Psoriasis 47 0.044
140
SYN036 Syncope 46 0.044
141
TRN044 Transposition of the Great Arteries 46 0.044
142
STP004 Staphylococcal Toxic Shock Syndrome 45 0.044
143
OST004 Osteitis Fibrosa 45 0.044
144
LYM020 Lymph Node Cancer 44 0.044
145
P INT063 Intellectual Disability 44 0.044
146
GST071 Gastrointestinal Carcinoma 44 0.044
147
ATS008 Autosomal Dominant Disease 43 0.044
148
CLC001 Calciphylaxis 43 0.044
149
MNR003 Mineral Metabolism Disease 43 0.044
150
P ACT150 Acute Adrenal Insufficiency 43 0.044
151
INT088 Intrinsic Factor Deficiency 43 0.044
152
ETH004 Euthyroid Sick Syndrome 43 0.044
153
P HYP265 Hypotonia 43 0.044
154
CRT002 Cartilage-Hair Hypoplasia 43 0.044
155
P MLT008 Multinodular Goiter 41 0.044
156
OST008 Osteosclerotic Myeloma 41 0.044
157
P HYP057 Hypervitaminosis D 41 0.044
158
RNL078 Renal Dysplasia 41 0.044
159
SXD001 Sex Differentiation Disease 41 0.044
160
MDS022 Mediastinitis 40 0.044
161
PRN039 Paraneoplastic Syndromes 40 0.044
162
MDS018 Mediastinal Cancer 39 0.044
163
VSC018 Visceral Steatosis 39 0.044
164
IDP073 Idiopathic Hypercalciuria 39 0.044
165
c OST131 Osteopetrosis, Autosomal Dominant 2 39 0.044
166
MCR018 Microcytic Anemia 38 0.044
167
ORL022 Oral Erosive Lichen 38 0.044
168
STT004 Steatorrhea 37 0.044
169
JJN008 Jejunoileitis 36 0.044
170
c ACT053 Acute Thyroiditis 35 0.044
171
FTL007 Fetal Hydantoin Syndrome 35 0.044
172
TRC020 Tracheitis 34 0.044
173
P HYP534 Hypomagnesemia 3, Renal 33 0.044
174
HYP315 Hyperparathyroidism, Neonatal 33 0.044
175
c OST126 Osteopetrosis, Autosomal Recessive 1 32 0.044
176
VSC008 Vascular Hemostatic Disease 31 0.044
177
P HRT017 Heart Tumor 31 0.044
178
BNM008 Bone Mineral Density, Low 31 0.044
179
c PRM158 Primary Intestinal Lymphangiectasia 30 0.044
180
HYP347 Hypotonia-Cystinuria Syndrome 30 0.044
181
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 29 0.044
182
P RNL066 Renal Tubular Acidosis, Distal, Ad 28 0.044
183
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 25 0.044
184
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 24 0.044
185
c CRN214 Coronary Heart Disease 5 23 0.044
186
c PSD035 Pseudohypoparathyroidism Type 2 23 0.044
187
c CRN177 Coronary Heart Disease 7 22 0.044
188
c PSD058 Pseudohypoparathyroidism Ic 22 0.044
189
2P2001 2p21 Microdeletion Syndrome 19 0.044
190
c ADL079 Adult Heart Tumor 19 0.044
191
HYP666 Hypoparathyroidism-Deafness-Renal Disease Syndrome 16 0.044
192
FML229 Familial Cutaneous Collagenoma 16 0.044
193
HYP611 Hypoparathyroidism, X-Linked 15 0.044
194
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 15 0.044
195
c MYP088 Myopathy, Tubular Aggregate, 2 15 0.044
196
THY021 Thyroid Malformation 14 0.044
197
MLL020 Müllerian Derivatives-Lymphangiectasia-Polydactyly Syndrome 12 0.044
198
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.044
199
CRN156 Craniofacioskeletal Syndrome 11 0.044
200
CSR002 Casr-Related Disorders 4 0.044