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

162 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 52 7.388
2
HYP550 Hypomagnesemia 1, Intestinal 20 3.400
3
HYP132 Hypomagnesemia with Secondary Hypocalcemia 13 3.357
4
c HYP564 Hypocalcemia, Autosomal Dominant 2 14 3.302
5
HYP316 Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 9 3.302
6
c KNN005 Kenny-Caffey Syndrome Type 2 24 2.404
7
HYP025 Hyperphosphatemia 50 0.278
8
P HYP024 Hypoparathyroidism 58 0.240
9
c HYP069 Hyperparathyroidism 63 0.188
10
c PSD015 Pseudohypoparathyroidism 55 0.156
11
P BRT034 Bartter Syndrome, Type 2 42 0.149
12
P PRM005 Primary Hyperparathyroidism 72 0.133
13
HYP005 Hypokalemia 50 0.133
14
CSR002 Casr-Related Disorders 4 0.133
15
P GRV001 Graves' Disease 63 0.124
16
c FML068 Familial Hypocalciuric Hypercalcemia 22 0.124
17
HYP004 Hypercalcemia 69 0.115
18
P RCK004 Rickets 67 0.115
19
P DGR001 Digeorge Syndrome 67 0.115
20
THR013 Thoracic Outlet Syndrome 54 0.115
21
HYP017 Hypophosphatemia 53 0.115
22
P NPH009 Nephrolithiasis 59 0.105
23
P OCL041 Oculomotor Apraxia Cogan Type 18 0.105
24
P ALZ001 Alzheimer's Disease 103 0.094
25
P CLC005 Celiac Disease 73 0.094
26
OST011 Osteomalacia 57 0.094
27
c FML070 Familial Hypocalciuric Hypercalcemia Type 2 6 0.094
28
P HYP075 Hypertension 86 0.081
29
P DLT002 Dilated Cardiomyopathy 82 0.081
30
P LKM002 Leukemia 79 0.081
31
c THY032 Thyroiditis 67 0.081
32
c ACT073 Acute Leukemia 62 0.081
33
c HYP076 Hyperthyroidism 61 0.081
34
P OST001 Osteopetrosis 60 0.081
35
PRT029 Parathyroid Adenoma 56 0.081
36
ERL004 Early Yaws 33 0.081
37
HPT023 Hepatocellular Carcinoma 89 0.066
38
P MYC007 Myocardial Infarction 88 0.066
39
CNG034 Congestive Heart Failure 81 0.066
40
P OST002 Osteoporosis 77 0.066
41
c HPT021 Hepatitis 75 0.066
42
ACN002 Acanthosis Nigricans 73 0.066
43
ADN018 Adenoma 67 0.066
44
WST001 West Syndrome 64 0.066
45
BRN106 Burns 64 0.066
46
c ACT075 Acute Myocardial Infarction 61 0.066
47
c HPT003 Hepatitis a 60 0.066
48
P PTT014 Pitt-Hopkins Syndrome 59 0.066
49
c MYL007 Myeloma 59 0.066
50
c HYP065 Hyperaldosteronism 59 0.066
51
P LYM026 Lymphoblastic Leukemia 56 0.066
52
P THR090 Thrombocythemia 1 54 0.066
53
ADL002 Adult Syndrome 52 0.066
54
P PND001 Pain Disorder 49 0.066
55
c BRT004 Bartter Disease 49 0.066
56
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 47 0.066
57
c OPT004 Optic Atrophy 46 0.066
58
P OST051 Osteopetrosis Autosomal Recessive 1 46 0.066
59
IMP004 Impetigo 45 0.066
60
P VTM018 Vitamin D-Dependent Rickets Type I 43 0.066
61
P HYP216 Hypoparathyroidism Familial Isolated 43 0.066
62
SYN053 Syndromic Diarrhea 42 0.066
63
P BNC001 Bone Carcinoma 41 0.066
64
MYC033 Myoclonus 33 0.066
65
THY001 Thyroid Crisis 25 0.066
66
c ATM068 Autoimmune Hypoparathyroidism 21 0.066
67
IMP001 Impetigo Herpetiformis 19 0.066
68
P AMY001 Amyotrophic Lateral Sclerosis 100 0.047
69
VNH001 Von Hippel-Lindau Disease 89 0.047
70
P MLT019 Multiple Myeloma 89 0.047
71
P OST018 Osteosarcoma 81 0.047
72
ACR007 Acromegaly 80 0.047
73
c DBT009 Diabetes Mellitus 80 0.047
74
P PNM007 Pneumonia 79 0.047
75
P LPR003 Leprosy 78 0.047
76
ANX002 Anxiety Disorder 75 0.047
77
P PGT001 Paget's Disease of Bone 74 0.047
78
P CNG026 Congenital Heart Defect 73 0.047
79
SPN038 Spina Bifida 70 0.047
80
c BTT002 Beta Thalassemia 70 0.047
81
c OST005 Osteogenesis Imperfecta 70 0.047
82
P PRT010 Parathyroid Carcinoma 69 0.047
83
PSY004 Psychotic Disorder 69 0.047
84
c THL005 Thalassemia 68 0.047
85
c HYP086 Hypothyroidism 68 0.047
86
GTL001 Gitelman Syndrome 67 0.047
87
P MTB001 Metabolic Syndrome X 67 0.047
88
PRP030 Purpura 67 0.047
89
DFC004 Deficiency Anemia 66 0.047
90
P PLY019 Polyneuropathy 64 0.047
91
BRC012 Brucellosis 63 0.047
92
GST009 Gastroschisis 63 0.047
93
TXC005 Toxic Shock Syndrome 63 0.047
94
TYP007 Typhoid Fever 63 0.047
95
LPR001 Lepromatous Leprosy 62 0.047
96
P GTR002 Goiter 61 0.047
97
P INT068 Intestinal Disease 61 0.047
98
P HLP001 Holoprosencephaly 61 0.047
99
P VLC001 Velocardiofacial Syndrome 60 0.047
100
P ESN007 Eosinophilia 60 0.047
101
ALP008 Alopecia 60 0.047
102
PSR002 Psoriasis 60 0.047
103
ACT049 Acute Disseminated Encephalomyelitis 60 0.047
104
INT075 Intracranial Hypertension 59 0.047
105
THY033 Thyrotoxicosis 58 0.047
106
NRN001 Neuroendocrine Carcinoma 57 0.047
107
EPL002 Epilepsy Syndrome 57 0.047
108
URM002 Uremia 56 0.047
109
MDS022 Mediastinitis 56 0.047
110
CRT002 Cartilage-Hair Hypoplasia 56 0.047
111
RNL011 Renal Osteodystrophy 56 0.047
112
SPT005 Spotted Fever 55 0.047
113
LPC002 Lip Cancer 55 0.047
114
c DRR001 Diarrhea 54 0.047
115
NPH003 Nephrocalcinosis 53 0.047
116
P FNC004 Fanconi Syndrome 53 0.047
117
c OPH004 Ophthalmoplegia 52 0.047
118
CLC001 Calciphylaxis 52 0.047
119
P INT063 Intellectual Disability 51 0.047
120
MCR018 Microcytic Anemia 51 0.047
121
STT004 Steatorrhea 50 0.047
122
PLM010 Pulmonary Edema 50 0.047
123
OST004 Osteitis Fibrosa 49 0.047
124
SCH016 Schimke Immunoosseous Dysplasia 49 0.047
125
PRT019 Protein-Losing Enteropathy 48 0.047
126
DNG002 Dengue Hemorrhagic Fever 47 0.047
127
P MLT008 Multinodular Goiter 47 0.047
128
P ATX010 Ataxia Neuropathy Spectrum 44 0.047
129
ETH004 Euthyroid Sick Syndrome 44 0.047
130
NNT010 Nontoxic Goiter 44 0.047
131
TTR016 Tetra-Amelia Syndrome 43 0.047
132
c HYP057 Hypervitaminosis D 42 0.047
133
P CHL080 Cholestasis, Progressive Familial Intrahepatic 1 37 0.047
134
c INT191 Intestinal Lymphangiectasia 37 0.047
135
P AGM005 Agammaglobulinemia, X-Linked 1 36 0.047
136
c PSD033 Pseudohypoparathyroidism Type 1b 35 0.047
137
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 35 0.047
138
MNT147 Mental Retardation 35 0.047
139
HNN001 Hennekam Syndrome 35 0.047
140
RCK007 Rickets, Vitamin D-Resistant, Type Iia 34 0.047
141
TRC020 Tracheitis 33 0.047
142
c OST050 Osteopetrosis Autosomal Dominant Type 2 33 0.047
143
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 30 0.047
144
BRK004 Barakat Syndrome 30 0.047
145
P KNN004 Kenny-Caffey Syndrome Type 1 29 0.047
146
c 2P2001 2p21 Microdeletion Syndrome 29 0.047
147
c ACT053 Acute Thyroiditis 28 0.047
148
NTR005 Nutritional Deficiency Disease 28 0.047
149
DSS010 Dissociative Disorder 25 0.047
150
P PRM158 Primary Intestinal Lymphangiectasia 23 0.047
151
PRS063 Paresthesia 22 0.047
152
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 21 0.047
153
c ALP060 Alpha Heavy-Chain Disease 21 0.047
154
c BNG076 Benign Exophthalmos Syndrome 21 0.047
155
OST008 Osteosclerotic Myeloma 19 0.047
156
DHL001 Dahlberg Borer Newcomer Syndrome 18 0.047
157
c RNG005 Ring Chromosome 10 17 0.047
158
FML229 Familial Cutaneous Collagenoma 16 0.047
159
MLL014 Mullerian Derivatives - Lymphangiectasia - Polydactyly 15 0.047
160
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 13 0.047
161
SCN043 Secondary Intestinal Lymphangiectasia 13 0.047
162
DNN005 Dennis-Cohen Syndrome 8 0.047