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

180 hits were found for 'hypocalcemia'

# ++ Fam MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 45 7.481
2
HYP550 Hypomagnesemia 1, Intestinal 12 3.353
3
c HYP132 Hypomagnesemia with Secondary Hypocalcemia 11 3.353
4
c HYP564 Hypocalcemia, Autosomal Dominant 2 8 3.300
5
c HYP316 Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 3 3.300
6
c KNN005 Kenny-Caffey Syndrome Type 2 15 2.400
7
HYP025 Hyperphosphatemia 48 0.268
8
P HYP024 Hypoparathyroidism 57 0.231
9
c HYP069 Hyperparathyroidism 57 0.181
10
c PSD015 Pseudohypoparathyroidism 49 0.150
11
c FML068 Familial Hypocalciuric Hypercalcemia 31 0.150
12
c BRT034 Bartter Syndrome, Type 2 34 0.143
13
P PRM005 Primary Hyperparathyroidism 66 0.128
14
HYP005 Hypokalemia 50 0.128
15
CSR002 Casr-Related Disorders 3 0.128
16
P GRV001 Graves' Disease 63 0.120
17
HYP004 Hypercalcemia 69 0.111
18
P RCK004 Rickets 65 0.111
19
P DGR001 Digeorge Syndrome 60 0.111
20
THR013 Thoracic Outlet Syndrome 53 0.111
21
HYP017 Hypophosphatemia 52 0.111
22
RPD005 Rapidly Involuting Congenital Hemangioma 19 0.111
23
P NPH009 Nephrolithiasis 57 0.101
24
P OCL041 Oculomotor Apraxia Cogan Type 17 0.101
25
P HYP211 Hypomagnesemia Primary 11 0.101
26
P ALZ001 Alzheimer's Disease 93 0.091
27
P CLC005 Celiac Disease 71 0.091
28
ACN002 Acanthosis Nigricans 70 0.091
29
OST011 Osteomalacia 56 0.091
30
c HYP314 Hypocalciuric Hypercalcemia, Type I 20 0.091
31
c FML070 Familial Hypocalciuric Hypercalcemia Type 2 5 0.091
32
P HYP075 Hypertension 76 0.079
33
P DLT002 Dilated Cardiomyopathy 74 0.079
34
LKM002 Leukemia 70 0.079
35
ACT073 Acute Leukemia 62 0.079
36
P OST001 Osteopetrosis 59 0.079
37
c HYP076 Hyperthyroidism 55 0.079
38
P PRT029 Parathyroid Adenoma 49 0.079
39
c ERL004 Early Yaws 29 0.079
40
P MYC007 Myocardial Infarction 82 0.064
41
CNG034 Congestive Heart Failure 74 0.064
42
P OST002 Osteoporosis 73 0.064
43
HPT023 Hepatocellular Carcinoma 69 0.064
44
ADN018 Adenoma 67 0.064
45
WST001 West Syndrome 64 0.064
46
SPT013 Septic Shock 62 0.064
47
c THY032 Thyroiditis 61 0.064
48
c ACT075 Acute Myocardial Infarction 59 0.064
49
GTL001 Gitelman Syndrome 54 0.064
50
c MYL007 Myeloma 53 0.064
51
ADL002 Adult Syndrome 50 0.064
52
LYM026 Lymphoblastic Leukemia 49 0.064
53
P PND001 Pain Disorder 49 0.064
54
P PTT014 Pitt-Hopkins Syndrome 49 0.064
55
P THR090 Thrombocythemia 1 48 0.064
56
P BRT004 Bartter Disease 48 0.064
57
MYC033 Myoclonus 47 0.064
58
INT191 Intestinal Lymphangiectasia 43 0.064
59
IMP004 Impetigo 41 0.064
60
c OPT004 Optic Atrophy 41 0.064
61
BNC001 Bone Carcinoma 39 0.064
62
P OST051 Osteopetrosis Autosomal Recessive 1 38 0.064
63
P VTM018 Vitamin D-Dependent Rickets Type I 36 0.064
64
OP3001 Opa3-Related 3-Methylglutaconic Aciduria 36 0.064
65
P HYP216 Hypoparathyroidism Familial Isolated 35 0.064
66
c ATX010 Ataxia Neuropathy Spectrum 33 0.064
67
c ATM068 Autoimmune Hypoparathyroidism 25 0.064
68
THY001 Thyroid Crisis 24 0.064
69
P HYP315 Hyperparathyroidism, Neonatal 20 0.064
70
IMP001 Impetigo Herpetiformis 19 0.064
71
P AMY001 Amyotrophic Lateral Sclerosis 87 0.045
72
P MLT019 Multiple Myeloma 76 0.045
73
ACR007 Acromegaly 75 0.045
74
ANX002 Anxiety Disorder 73 0.045
75
P OST018 Osteosarcoma 70 0.045
76
THL005 Thalassemia 69 0.045
77
BTT002 Beta Thalassemia 69 0.045
78
P OST005 Osteogenesis Imperfecta 69 0.045
79
c DBT009 Diabetes Mellitus 68 0.045
80
P PNM007 Pneumonia 67 0.045
81
P LPR003 Leprosy 67 0.045
82
P HPT001 Hepatitis C 66 0.045
83
P CNG026 Congenital Heart Defect 65 0.045
84
DFC004 Deficiency Anemia 65 0.045
85
c HPT021 Hepatitis 65 0.045
86
SPN038 Spina Bifida 63 0.045
87
PRT010 Parathyroid Carcinoma 63 0.045
88
PSY004 Psychotic Disorder 62 0.045
89
P HLP001 Holoprosencephaly 61 0.045
90
BRN106 Burns 61 0.045
91
PRP030 Purpura 60 0.045
92
TXC005 Toxic Shock Syndrome 60 0.045
93
TYP007 Typhoid Fever 60 0.045
94
c HPT015 Hepatitis D 59 0.045
95
LPR001 Lepromatous Leprosy 59 0.045
96
ALP008 Alopecia 59 0.045
97
c HYP086 Hypothyroidism 59 0.045
98
HMR012 Hemorrhagic Fever 58 0.045
99
MLT074 Multiple Endocrine Neoplasia 58 0.045
100
GST009 Gastroschisis 58 0.045
101
P VLC001 Velocardiofacial Syndrome 57 0.045
102
NSY001 N Syndrome 57 0.045
103
ACT049 Acute Disseminated Encephalomyelitis 56 0.045
104
P GTR002 Goiter 55 0.045
105
NRN001 Neuroendocrine Carcinoma 55 0.045
106
THY033 Thyrotoxicosis 55 0.045
107
URM002 Uremia 54 0.045
108
P PLY019 Polyneuropathy 54 0.045
109
P ESN007 Eosinophilia 54 0.045
110
c MYL014 Myeloproliferative Disorder 54 0.045
111
INT075 Intracranial Hypertension 53 0.045
112
P EPL002 Epilepsy Syndrome 52 0.045
113
BRC012 Brucellosis 52 0.045
114
P FNC004 Fanconi Syndrome 52 0.045
115
NPH003 Nephrocalcinosis 52 0.045
116
PSR002 Psoriasis 51 0.045
117
MYL020 Myelomeningocele 51 0.045
118
SPT005 Spotted Fever 51 0.045
119
c MNT147 Mental Retardation 51 0.045
120
P INT068 Intestinal Disease 51 0.045
121
LPC002 Lip Cancer 50 0.045
122
c HYP065 Hyperaldosteronism 50 0.045
123
RNL011 Renal Osteodystrophy 50 0.045
124
PLM010 Pulmonary Edema 50 0.045
125
CRT002 Cartilage-Hair Hypoplasia 50 0.045
126
P CLC001 Calciphylaxis 49 0.045
127
STT004 Steatorrhea 49 0.045
128
SYN036 Syncope 49 0.045
129
c DRR001 Diarrhea 49 0.045
130
RNL078 Renal Dysplasia 47 0.045
131
MCR018 Microcytic Anemia 46 0.045
132
c OPH004 Ophthalmoplegia 46 0.045
133
PRT019 Protein-Losing Enteropathy 46 0.045
134
c MLT008 Multinodular Goiter 46 0.045
135
OST004 Osteitis Fibrosa 46 0.045
136
PRN039 Paraneoplastic Syndromes 45 0.045
137
DNG002 Dengue Hemorrhagic Fever 45 0.045
138
HYP265 Hypotonia 43 0.045
139
CHR101 Char Syndrome 42 0.045
140
INT063 Intellectual Disability 42 0.045
141
NNT010 Nontoxic Goiter 41 0.045
142
c HYP057 Hypervitaminosis D 41 0.045
143
ETH004 Euthyroid Sick Syndrome 40 0.045
144
FTL007 Fetal Hydantoin Syndrome 40 0.045
145
SZR006 Seizure Disorder 40 0.045
146
SCH016 Schimke Immunoosseous Dysplasia 40 0.045
147
STP004 Staphylococcal Toxic Shock Syndrome 39 0.045
148
c ACT150 Acute Adrenal Insufficiency 37 0.045
149
TTR016 Tetra-Amelia Syndrome 36 0.045
150
YNG002 Young Syndrome 34 0.045
151
DYS036 Dysequilibrium Syndrome 32 0.045
152
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 32 0.045
153
PRS063 Paresthesia 32 0.045
154
PRX035 Paroxysmal Dyskinesia 32 0.045
155
TRC020 Tracheitis 32 0.045
156
INT088 Intrinsic Factor Deficiency 29 0.045
157
P PSD033 Pseudohypoparathyroidism Type 1b 28 0.045
158
HNN001 Hennekam Syndrome 28 0.045
159
P CHL080 Cholestasis, Progressive Familial Intrahepatic 1 27 0.045
160
BRK004 Barakat Syndrome 27 0.045
161
PRM158 Primary Intestinal Lymphangiectasia 25 0.045
162
c 2P2001 2p21 Microdeletion Syndrome 25 0.045
163
c ACT053 Acute Thyroiditis 25 0.045
164
P AGM005 Agammaglobulinemia, X-Linked 1 25 0.045
165
P KNN004 Kenny-Caffey Syndrome Type 1 24 0.045
166
c ALP060 Alpha Heavy-Chain Disease 23 0.045
167
RCK007 Rickets, Vitamin D-Resistant, Type Iia 23 0.045
168
c OST050 Osteopetrosis Autosomal Dominant Type 2 23 0.045
169
c HYP329 Hypoparathyroidism, Autosomal Dominant 21 0.045
170
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 19 0.045
171
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 18 0.045
172
c BNG076 Benign Exophthalmos Syndrome 17 0.045
173
OST008 Osteosclerotic Myeloma 15 0.045
174
FML229 Familial Cutaneous Collagenoma 15 0.045
175
c RNG005 Ring Chromosome 10 14 0.045
176
SCN043 Secondary Intestinal Lymphangiectasia 13 0.045
177
DHL001 Dahlberg Borer Newcomer Syndrome 13 0.045
178
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 9 0.045
179
MLL014 Mullerian Derivatives - Lymphangiectasia - Polydactyly 8 0.045
180
DNN005 Dennis-Cohen Syndrome 6 0.045