Search results for "hypocalcemia"

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

167 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 53 7.111
2
HYP132 Hypomagnesemia with Secondary Hypocalcemia 22 4.297
3
HYP550 Hypomagnesemia 1, Intestinal 20 3.385
4
HYP316 Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 10 3.308
5
c HYP564 Hypocalcemia, Autosomal Dominant 2 9 3.308
6
P KNN005 Kenny-Caffey Syndrome Type 2 29 2.433
7
HYP025 Hyperphosphatemia 43 0.276
8
P HYP024 Hypoparathyroidism 57 0.243
9
c HYP069 Hyperparathyroidism 65 0.181
10
c PSD015 Pseudohypoparathyroidism 55 0.155
11
P PRM005 Primary Hyperparathyroidism 71 0.132
12
HYP005 Hypokalemia 50 0.132
13
P GRV001 Graves' Disease 51 0.124
14
P RCK004 Rickets 68 0.114
15
HYP004 Hypercalcemia 65 0.114
16
HYP017 Hypophosphatemia 49 0.114
17
P CLC005 Celiac Disease 73 0.093
18
P DGR001 Digeorge Syndrome 67 0.093
19
P OST001 Osteopetrosis 66 0.093
20
c FML068 Familial Hypocalciuric Hypercalcemia 38 0.093
21
P DLT002 Dilated Cardiomyopathy 88 0.081
22
P HYP075 Hypertension 87 0.081
23
P LKM002 Leukemia 77 0.081
24
c THY032 Thyroiditis 66 0.081
25
c HYP076 Hyperthyroidism 64 0.081
26
OST011 Osteomalacia 53 0.081
27
P SZR006 Seizure Disorder 51 0.081
28
P MYC007 Myocardial Infarction 93 0.066
29
CNG034 Congestive Heart Failure 78 0.066
30
ADN018 Adenoma 66 0.066
31
c HPT021 Hepatitis 64 0.066
32
P ACT101 Acute Lymphoblastic Leukemia 63 0.066
33
c MYL007 Myeloma 61 0.066
34
c ACT075 Acute Myocardial Infarction 60 0.066
35
CRT002 Cartilage-Hair Hypoplasia 60 0.066
36
P PTT014 Pitt-Hopkins Syndrome 59 0.066
37
c HYP065 Hyperaldosteronism 58 0.066
38
c LYM026 Lymphoblastic Leukemia 57 0.066
39
c BRT004 Bartter Disease 54 0.066
40
PRT029 Parathyroid Adenoma 53 0.066
41
THR013 Thoracic Outlet Syndrome 52 0.066
42
c DRR001 Diarrhea 52 0.066
43
BRN106 Burns 50 0.066
44
IMP004 Impetigo 49 0.066
45
P VTM018 Vitamin D-Dependent Rickets Type I 45 0.066
46
P HYP216 Hypoparathyroidism Familial Isolated 43 0.066
47
P BRT034 Bartter Syndrome, Type 2 40 0.066
48
SYN053 Syndromic Diarrhea 34 0.066
49
THY001 Thyroid Crisis 28 0.066
50
IMP001 Impetigo Herpetiformis 23 0.066
51
P ALZ001 Alzheimer's Disease 100 0.047
52
P LVR011 Liver Cancer 91 0.047
53
P MLT019 Multiple Myeloma 88 0.047
54
P OST018 Osteosarcoma 82 0.047
55
VNH001 Von Hippel-Lindau Disease 81 0.047
56
ACR007 Acromegaly 80 0.047
57
c BTT002 Beta Thalassemia 78 0.047
58
P LPR003 Leprosy 78 0.047
59
P PNM007 Pneumonia 78 0.047
60
P OST002 Osteoporosis 76 0.047
61
PGT001 Paget's Disease of Bone 75 0.047
62
c DBT009 Diabetes Mellitus 74 0.047
63
c OST005 Osteogenesis Imperfecta 74 0.047
64
c THL005 Thalassemia 72 0.047
65
GTL001 Gitelman Syndrome 70 0.047
66
c HYP086 Hypothyroidism 69 0.047
67
c AMY001 Amyotrophic Lateral Sclerosis 67 0.047
68
ACT049 Acute Disseminated Encephalomyelitis 67 0.047
69
GST009 Gastroschisis 66 0.047
70
PRP030 Purpura 66 0.047
71
c HLP001 Holoprosencephaly 64 0.047
72
P VLC001 Velocardiofacial Syndrome 64 0.047
73
ACN002 Acanthosis Nigricans 63 0.047
74
PSR002 Psoriasis 63 0.047
75
DFC004 Deficiency Anemia 63 0.047
76
P ESN007 Eosinophilia 63 0.047
77
P GTR002 Goiter 62 0.047
78
P PRT010 Parathyroid Carcinoma 62 0.047
79
P MYP004 Myopathy 62 0.047
80
TYP007 Typhoid Fever 62 0.047
81
TXC005 Toxic Shock Syndrome 62 0.047
82
c MLT074 Multiple Endocrine Neoplasia 61 0.047
83
P PLY019 Polyneuropathy 61 0.047
84
BRC012 Brucellosis 61 0.047
85
SPT013 Septic Shock 61 0.047
86
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.047
87
c HPT003 Hepatitis a 59 0.047
88
NRN001 Neuroendocrine Carcinoma 59 0.047
89
P NPH009 Nephrolithiasis 58 0.047
90
URM002 Uremia 58 0.047
91
P INT068 Intestinal Disease 58 0.047
92
THY033 Thyrotoxicosis 58 0.047
93
P HMR012 Hemorrhagic Fever 58 0.047
94
ALP008 Alopecia 57 0.047
95
c ACT073 Acute Leukemia 57 0.047
96
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 56 0.047
97
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.047
98
CLC001 Calciphylaxis 56 0.047
99
OST004 Osteitis Fibrosa 55 0.047
100
STT004 Steatorrhea 54 0.047
101
JHN001 Johanson-Blizzard Syndrome 53 0.047
102
c OPH004 Ophthalmoplegia 53 0.047
103
INT075 Intracranial Hypertension 53 0.047
104
SPT005 Spotted Fever 53 0.047
105
MNT147 Mental Retardation 52 0.047
106
P PND001 Pain Disorder 52 0.047
107
CRN014 Cronkhite-Canada Syndrome 52 0.047
108
RNL011 Renal Osteodystrophy 51 0.047
109
MNN014 Mononeuritis 51 0.047
110
PRT019 Protein-Losing Enteropathy 51 0.047
111
LPR001 Lepromatous Leprosy 51 0.047
112
P FNC004 Fanconi Syndrome 50 0.047
113
c OPT004 Optic Atrophy 50 0.047
114
DNG002 Dengue Hemorrhagic Fever 49 0.047
115
TRN044 Transposition of the Great Arteries 49 0.047
116
MDT001 Mediterranean Spotted Fever 49 0.047
117
NPH003 Nephrocalcinosis 49 0.047
118
c ACT150 Acute Adrenal Insufficiency 49 0.047
119
PLM010 Pulmonary Edema 49 0.047
120
P MLT008 Multinodular Goiter 48 0.047
121
c RNL078 Renal Dysplasia 48 0.047
122
SCH016 Schimke Immunoosseous Dysplasia 47 0.047
123
ETH004 Euthyroid Sick Syndrome 47 0.047
124
PRN039 Paraneoplastic Syndromes 47 0.047
125
STP004 Staphylococcal Toxic Shock Syndrome 46 0.047
126
MDS022 Mediastinitis 46 0.047
127
MCR018 Microcytic Anemia 46 0.047
128
P PSD033 Pseudohypoparathyroidism Type 1b 46 0.047
129
MYC033 Myoclonus 45 0.047
130
FTL007 Fetal Hydantoin Syndrome 45 0.047
131
SYN036 Syncope 44 0.047
132
P CHL080 Cholestasis, Progressive Familial Intrahepatic 1 43 0.047
133
INT088 Intrinsic Factor Deficiency 43 0.047
134
c HYP057 Hypervitaminosis D 43 0.047
135
P ATX010 Ataxia Neuropathy Spectrum 43 0.047
136
TTR016 Tetra-Amelia Syndrome 42 0.047
137
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.047
138
P OST052 Osteopetrosis Autosomal Recessive 2 42 0.047
139
HYP265 Hypotonia 41 0.047
140
PRS063 Paresthesia 36 0.047
141
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 35 0.047
142
BRK004 Barakat Syndrome 33 0.047
143
NTR005 Nutritional Deficiency Disease 33 0.047
144
TRC020 Tracheitis 33 0.047
145
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 31 0.047
146
c OST050 Osteopetrosis Autosomal Dominant Type 2 30 0.047
147
PRM158 Primary Intestinal Lymphangiectasia 30 0.047
148
c ATM068 Autoimmune Hypoparathyroidism 30 0.047
149
c ALP060 Alpha Heavy-Chain Disease 30 0.047
150
RCK007 Rickets, Vitamin D-Resistant, Type Iia 28 0.047
151
c OST051 Osteopetrosis Autosomal Recessive 1 26 0.047
152
c 2P2001 2p21 Microdeletion Syndrome 26 0.047
153
c ACT053 Acute Thyroiditis 25 0.047
154
JJN008 Jejunoileitis 24 0.047
155
c TBL012 Tubular Aggregate Myopathy 23 0.047
156
c RNG005 Ring Chromosome 10 22 0.047
157
c BNG076 Benign Exophthalmos Syndrome 22 0.047
158
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 22 0.047
159
FML229 Familial Cutaneous Collagenoma 21 0.047
160
P OCL041 Oculomotor Apraxia Cogan Type 20 0.047
161
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 19 0.047
162
DHL001 Dahlberg Borer Newcomer Syndrome 18 0.047
163
OST008 Osteosclerotic Myeloma 18 0.047
164
MLL017 Müllerian Derivatives - Lymphangiectasia - Polydactyly 15 0.047
165
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 15 0.047
166
SCN043 Secondary Intestinal Lymphangiectasia 12 0.047
167
CSR002 Casr-Related Disorders 5 0.047