Search results for "hypocalcemia"

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

161 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 53 7.109
2
HYP132 Hypomagnesemia with Secondary Hypocalcemia 22 3.562
3
HYP550 Hypomagnesemia 1, Intestinal 19 3.384
4
c HYP564 Hypocalcemia, Autosomal Dominant 2 10 3.307
5
HYP316 Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 10 3.307
6
c KNN005 Kenny-Caffey Syndrome Type 2 20 2.407
7
HYP025 Hyperphosphatemia 42 0.275
8
P HYP024 Hypoparathyroidism 57 0.236
9
c HYP069 Hyperparathyroidism 64 0.183
10
c PSD015 Pseudohypoparathyroidism 54 0.157
11
P PRM005 Primary Hyperparathyroidism 68 0.133
12
HYP005 Hypokalemia 47 0.133
13
P GRV001 Graves' Disease 64 0.125
14
P RCK004 Rickets 64 0.116
15
HYP017 Hypophosphatemia 48 0.116
16
P DGR001 Digeorge Syndrome 67 0.106
17
HYP004 Hypercalcemia 65 0.106
18
P CLC005 Celiac Disease 74 0.094
19
c FML068 Familial Hypocalciuric Hypercalcemia 37 0.094
20
P HYP075 Hypertension 85 0.082
21
P DLT002 Dilated Cardiomyopathy 82 0.082
22
P LKM002 Leukemia 77 0.082
23
c THY032 Thyroiditis 66 0.082
24
P OST001 Osteopetrosis 63 0.082
25
c HYP076 Hyperthyroidism 62 0.082
26
OST011 Osteomalacia 52 0.082
27
P MYC007 Myocardial Infarction 92 0.067
28
CNG034 Congestive Heart Failure 78 0.067
29
c HPT021 Hepatitis 64 0.067
30
ADN018 Adenoma 64 0.067
31
c MYL007 Myeloma 61 0.067
32
c ACT075 Acute Myocardial Infarction 59 0.067
33
P PTT014 Pitt-Hopkins Syndrome 59 0.067
34
c HYP065 Hyperaldosteronism 57 0.067
35
c LYM026 Lymphoblastic Leukemia 54 0.067
36
PRT029 Parathyroid Adenoma 52 0.067
37
THR013 Thoracic Outlet Syndrome 52 0.067
38
IMP004 Impetigo 51 0.067
39
c DRR001 Diarrhea 51 0.067
40
c BRT004 Bartter Disease 51 0.067
41
c INT191 Intestinal Lymphangiectasia 50 0.067
42
BRN106 Burns 49 0.067
43
P OST051 Osteopetrosis Autosomal Recessive 1 45 0.067
44
P VTM018 Vitamin D-Dependent Rickets Type I 44 0.067
45
P HYP216 Hypoparathyroidism Familial Isolated 41 0.067
46
c BRT034 Bartter Syndrome, Type 2 34 0.067
47
SYN053 Syndromic Diarrhea 32 0.067
48
THY001 Thyroid Crisis 26 0.067
49
IMP001 Impetigo Herpetiformis 23 0.067
50
P AMY001 Amyotrophic Lateral Sclerosis 98 0.047
51
P ALZ001 Alzheimer's Disease 97 0.047
52
P MLT019 Multiple Myeloma 82 0.047
53
VNH001 Von Hippel-Lindau Disease 80 0.047
54
HPT023 Hepatocellular Carcinoma 79 0.047
55
P OST018 Osteosarcoma 79 0.047
56
ACR007 Acromegaly 79 0.047
57
c DBT009 Diabetes Mellitus 78 0.047
58
P LPR003 Leprosy 77 0.047
59
c BTT002 Beta Thalassemia 77 0.047
60
P PNM007 Pneumonia 76 0.047
61
P OST002 Osteoporosis 75 0.047
62
P PGT001 Paget's Disease of Bone 72 0.047
63
c OST005 Osteogenesis Imperfecta 72 0.047
64
c THL005 Thalassemia 72 0.047
65
ACN002 Acanthosis Nigricans 69 0.047
66
c HYP086 Hypothyroidism 69 0.047
67
SPN038 Spina Bifida 67 0.047
68
GST009 Gastroschisis 66 0.047
69
PRP030 Purpura 64 0.047
70
GTL001 Gitelman Syndrome 64 0.047
71
P HLP001 Holoprosencephaly 64 0.047
72
ACT049 Acute Disseminated Encephalomyelitis 63 0.047
73
P VLC001 Velocardiofacial Syndrome 63 0.047
74
PSR002 Psoriasis 63 0.047
75
DFC004 Deficiency Anemia 62 0.047
76
P PRT010 Parathyroid Carcinoma 62 0.047
77
P GTR002 Goiter 62 0.047
78
P ESN007 Eosinophilia 61 0.047
79
MYL020 Myelomeningocele 61 0.047
80
TXC005 Toxic Shock Syndrome 61 0.047
81
TYP007 Typhoid Fever 60 0.047
82
c HMR012 Hemorrhagic Fever 60 0.047
83
P PLY019 Polyneuropathy 60 0.047
84
BRC012 Brucellosis 60 0.047
85
SPT013 Septic Shock 60 0.047
86
c MLT074 Multiple Endocrine Neoplasia 59 0.047
87
c HPT003 Hepatitis a 59 0.047
88
P INT068 Intestinal Disease 58 0.047
89
NRN001 Neuroendocrine Carcinoma 58 0.047
90
P NPH009 Nephrolithiasis 57 0.047
91
ALP008 Alopecia 56 0.047
92
c ACT073 Acute Leukemia 56 0.047
93
URM002 Uremia 56 0.047
94
CRT002 Cartilage-Hair Hypoplasia 56 0.047
95
CLC001 Calciphylaxis 55 0.047
96
OST004 Osteitis Fibrosa 54 0.047
97
STT004 Steatorrhea 54 0.047
98
c OPH004 Ophthalmoplegia 53 0.047
99
SPT005 Spotted Fever 52 0.047
100
c MYL014 Myeloproliferative Disorder 52 0.047
101
INT075 Intracranial Hypertension 51 0.047
102
MNT147 Mental Retardation 51 0.047
103
RNL011 Renal Osteodystrophy 51 0.047
104
PRT019 Protein-Losing Enteropathy 50 0.047
105
LPR001 Lepromatous Leprosy 50 0.047
106
c OPT004 Optic Atrophy 50 0.047
107
P INT063 Intellectual Disability 50 0.047
108
P FNC004 Fanconi Syndrome 49 0.047
109
DNG002 Dengue Hemorrhagic Fever 49 0.047
110
TRN044 Transposition of the Great Arteries 49 0.047
111
P PND001 Pain Disorder 48 0.047
112
c ACT150 Acute Adrenal Insufficiency 48 0.047
113
NPH003 Nephrocalcinosis 48 0.047
114
PLM010 Pulmonary Edema 48 0.047
115
MDT001 Mediterranean Spotted Fever 48 0.047
116
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 47 0.047
117
c RNL078 Renal Dysplasia 47 0.047
118
ETH004 Euthyroid Sick Syndrome 47 0.047
119
STP004 Staphylococcal Toxic Shock Syndrome 46 0.047
120
PRN039 Paraneoplastic Syndromes 46 0.047
121
MCR018 Microcytic Anemia 46 0.047
122
SCH016 Schimke Immunoosseous Dysplasia 46 0.047
123
MDS022 Mediastinitis 46 0.047
124
P MLT008 Multinodular Goiter 45 0.047
125
MYC033 Myoclonus 45 0.047
126
FTL007 Fetal Hydantoin Syndrome 44 0.047
127
P PSD033 Pseudohypoparathyroidism Type 1b 44 0.047
128
SYN036 Syncope 44 0.047
129
INT088 Intrinsic Factor Deficiency 43 0.047
130
P SZR006 Seizure Disorder 43 0.047
131
TTR016 Tetra-Amelia Syndrome 41 0.047
132
P ATX010 Ataxia Neuropathy Spectrum 41 0.047
133
c HYP057 Hypervitaminosis D 41 0.047
134
HYP265 Hypotonia 41 0.047
135
HNN001 Hennekam Syndrome 39 0.047
136
PRS063 Paresthesia 35 0.047
137
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 35 0.047
138
TRC020 Tracheitis 33 0.047
139
BRK004 Barakat Syndrome 32 0.047
140
c OST050 Osteopetrosis Autosomal Dominant Type 2 31 0.047
141
c ATM068 Autoimmune Hypoparathyroidism 30 0.047
142
P KNN004 Kenny-Caffey Syndrome Type 1 30 0.047
143
P PRM158 Primary Intestinal Lymphangiectasia 30 0.047
144
c ALP060 Alpha Heavy-Chain Disease 29 0.047
145
RCK007 Rickets, Vitamin D-Resistant, Type Iia 29 0.047
146
c CHL083 Cholestasis, Progressive Familial Intrahepatic 4 28 0.047
147
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 27 0.047
148
c 2P2001 2p21 Microdeletion Syndrome 26 0.047
149
c ACT053 Acute Thyroiditis 26 0.047
150
NTR005 Nutritional Deficiency Disease 25 0.047
151
c RNG005 Ring Chromosome 10 23 0.047
152
c BNG076 Benign Exophthalmos Syndrome 22 0.047
153
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 21 0.047
154
FML229 Familial Cutaneous Collagenoma 20 0.047
155
P OCL041 Oculomotor Apraxia Cogan Type 20 0.047
156
OST008 Osteosclerotic Myeloma 19 0.047
157
DHL001 Dahlberg Borer Newcomer Syndrome 18 0.047
158
SCN043 Secondary Intestinal Lymphangiectasia 15 0.047
159
MLL017 Müllerian Derivatives - Lymphangiectasia - Polydactyly 15 0.047
160
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 14 0.047
161
CSR002 Casr-Related Disorders 5 0.047