Search results for "hypocalcemia"

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

176 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 54 7.116
2
HYP132 Hypomagnesemia with Secondary Hypocalcemia 22 4.290
3
HYP550 Hypomagnesemia 1, Intestinal 22 3.401
4
c HYP564 Hypocalcemia, Autosomal Dominant 2 11 3.335
5
HYP316 Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 9 3.306
6
P KNN005 Kenny-Caffey Syndrome Type 2 30 2.471
7
HYP025 Hyperphosphatemia 43 0.271
8
P HYP024 Hypoparathyroidism 57 0.238
9
c HYP069 Hyperparathyroidism 64 0.178
10
c PSD015 Pseudohypoparathyroidism 54 0.152
11
P PRM005 Primary Hyperparathyroidism 70 0.130
12
HYP005 Hypokalemia 49 0.130
13
P GRV001 Graves' Disease 64 0.121
14
P RCK004 Rickets 67 0.112
15
P DGR001 Digeorge Syndrome 67 0.112
16
HYP004 Hypercalcemia 64 0.112
17
HYP017 Hypophosphatemia 48 0.112
18
P CLC005 Celiac Disease 74 0.103
19
c OST001 Osteopetrosis 75 0.092
20
P HYP216 Hypoparathyroidism Familial Isolated 44 0.092
21
c FML068 Familial Hypocalciuric Hypercalcemia 38 0.092
22
P DLT002 Dilated Cardiomyopathy 87 0.079
23
P HYP075 Hypertension 85 0.079
24
P LKM002 Leukemia 76 0.079
25
P VLC001 Velocardiofacial Syndrome 66 0.079
26
c THY032 Thyroiditis 65 0.079
27
c HYP076 Hyperthyroidism 62 0.079
28
OST011 Osteomalacia 52 0.079
29
P SZR006 Seizure Disorder 50 0.079
30
MLL017 Müllerian Derivatives - Lymphangiectasia - Polydactyly 16 0.079
31
P MYC007 Myocardial Infarction 92 0.065
32
CNG034 Congestive Heart Failure 77 0.065
33
ADN018 Adenoma 65 0.065
34
P ACT101 Acute Lymphoblastic Leukemia 64 0.065
35
c HPT021 Hepatitis 63 0.065
36
c MYL007 Myeloma 60 0.065
37
P PTT014 Pitt-Hopkins Syndrome 59 0.065
38
c ACT075 Acute Myocardial Infarction 59 0.065
39
CRT002 Cartilage-Hair Hypoplasia 57 0.065
40
c HYP065 Hyperaldosteronism 57 0.065
41
c LYM026 Lymphoblastic Leukemia 56 0.065
42
c BRT004 Bartter Disease 53 0.065
43
THR013 Thoracic Outlet Syndrome 52 0.065
44
PRT029 Parathyroid Adenoma 52 0.065
45
c DRR001 Diarrhea 51 0.065
46
BRN106 Burns 49 0.065
47
P VTM018 Vitamin D-Dependent Rickets Type I 49 0.065
48
IMP004 Impetigo 49 0.065
49
P PSD033 Pseudohypoparathyroidism Type 1b 47 0.065
50
P CHL080 Cholestasis, Progressive Familial Intrahepatic 1 44 0.065
51
P BRT034 Bartter Syndrome, Type 2 43 0.065
52
P OST052 Osteopetrosis Autosomal Recessive 2 42 0.065
53
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 36 0.065
54
BRK004 Barakat Syndrome 34 0.065
55
SYN053 Syndromic Diarrhea 34 0.065
56
P HNN005 Hennekam Lymphangiectasia-Lymphedema Syndrome 1 33 0.065
57
c OST050 Osteopetrosis Autosomal Dominant Type 2 31 0.065
58
PRM158 Primary Intestinal Lymphangiectasia 31 0.065
59
c ALP060 Alpha Heavy-Chain Disease 30 0.065
60
RCK007 Rickets, Vitamin D-Resistant, Type Iia 29 0.065
61
THY001 Thyroid Crisis 27 0.065
62
c 2P2001 2p21 Microdeletion Syndrome 27 0.065
63
c RNG005 Ring Chromosome 10 23 0.065
64
IMP001 Impetigo Herpetiformis 23 0.065
65
FML229 Familial Cutaneous Collagenoma 21 0.065
66
DHL001 Dahlberg Borer Newcomer Syndrome 20 0.065
67
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 15 0.065
68
SCN043 Secondary Intestinal Lymphangiectasia 12 0.065
69
P ALZ001 Alzheimer's Disease 98 0.046
70
P LVR011 Liver Cancer 90 0.046
71
P MLT019 Multiple Myeloma 88 0.046
72
c BTT002 Beta Thalassemia 82 0.046
73
P OST018 Osteosarcoma 81 0.046
74
VNH001 Von Hippel-Lindau Disease 81 0.046
75
ACR007 Acromegaly 79 0.046
76
P LPR003 Leprosy 77 0.046
77
P PNM007 Pneumonia 77 0.046
78
PGT001 Paget's Disease of Bone 76 0.046
79
P OST002 Osteoporosis 76 0.046
80
c DBT009 Diabetes Mellitus 73 0.046
81
GTL001 Gitelman Syndrome 73 0.046
82
c OST005 Osteogenesis Imperfecta 72 0.046
83
c THL005 Thalassemia 71 0.046
84
c HYP086 Hypothyroidism 68 0.046
85
c HLP001 Holoprosencephaly 68 0.046
86
c AMY001 Amyotrophic Lateral Sclerosis 66 0.046
87
GST009 Gastroschisis 66 0.046
88
ACT049 Acute Disseminated Encephalomyelitis 66 0.046
89
CHR103 Charge Syndrome 65 0.046
90
PRP030 Purpura 65 0.046
91
ACN002 Acanthosis Nigricans 64 0.046
92
P PRT010 Parathyroid Carcinoma 64 0.046
93
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.046
94
PSR002 Psoriasis 62 0.046
95
DFC004 Deficiency Anemia 62 0.046
96
TYP007 Typhoid Fever 62 0.046
97
P ESN007 Eosinophilia 62 0.046
98
P GTR002 Goiter 61 0.046
99
P MYP004 Myopathy 61 0.046
100
TXC005 Toxic Shock Syndrome 61 0.046
101
c MLT074 Multiple Endocrine Neoplasia 60 0.046
102
P PLY019 Polyneuropathy 60 0.046
103
BRC012 Brucellosis 60 0.046
104
SPT013 Septic Shock 60 0.046
105
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.046
106
ALP008 Alopecia 59 0.046
107
P NPH009 Nephrolithiasis 59 0.046
108
c HPT003 Hepatitis a 58 0.046
109
NRN001 Neuroendocrine Carcinoma 58 0.046
110
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 57 0.046
111
URM002 Uremia 57 0.046
112
P INT068 Intestinal Disease 57 0.046
113
THY033 Thyrotoxicosis 57 0.046
114
P HMR012 Hemorrhagic Fever 57 0.046
115
c ACT073 Acute Leukemia 56 0.046
116
c MNT147 Mental Retardation 56 0.046
117
CLC001 Calciphylaxis 55 0.046
118
PRT019 Protein-Losing Enteropathy 55 0.046
119
JHN001 Johanson-Blizzard Syndrome 54 0.046
120
P PND001 Pain Disorder 54 0.046
121
OST004 Osteitis Fibrosa 54 0.046
122
c OPH004 Ophthalmoplegia 54 0.046
123
STT004 Steatorrhea 53 0.046
124
INT075 Intracranial Hypertension 52 0.046
125
CRN014 Cronkhite-Canada Syndrome 52 0.046
126
SPT005 Spotted Fever 52 0.046
127
RNL011 Renal Osteodystrophy 51 0.046
128
MNN014 Mononeuritis 51 0.046
129
LPR001 Lepromatous Leprosy 50 0.046
130
P FNC004 Fanconi Syndrome 50 0.046
131
c OPT004 Optic Atrophy 49 0.046
132
DNG002 Dengue Hemorrhagic Fever 49 0.046
133
TRN044 Transposition of the Great Arteries 49 0.046
134
MDT001 Mediterranean Spotted Fever 48 0.046
135
SCH016 Schimke Immunoosseous Dysplasia 48 0.046
136
NPH003 Nephrocalcinosis 48 0.046
137
c ACT150 Acute Adrenal Insufficiency 48 0.046
138
PLM010 Pulmonary Edema 48 0.046
139
P MLT008 Multinodular Goiter 47 0.046
140
c RNL078 Renal Dysplasia 47 0.046
141
P ATX010 Ataxia Neuropathy Spectrum 47 0.046
142
ETH004 Euthyroid Sick Syndrome 46 0.046
143
PRN039 Paraneoplastic Syndromes 46 0.046
144
STP004 Staphylococcal Toxic Shock Syndrome 46 0.046
145
MDS022 Mediastinitis 45 0.046
146
MCR018 Microcytic Anemia 45 0.046
147
INT088 Intrinsic Factor Deficiency 45 0.046
148
FTL007 Fetal Hydantoin Syndrome 45 0.046
149
MYC033 Myoclonus 44 0.046
150
SYN036 Syncope 44 0.046
151
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.046
152
TTR016 Tetra-Amelia Syndrome 43 0.046
153
c HYP057 Hypervitaminosis D 42 0.046
154
P CRN108 Cranioectodermal Dysplasia 1 42 0.046
155
HYP265 Hypotonia 40 0.046
156
VSC018 Visceral Steatosis 37 0.046
157
PRS063 Paresthesia 35 0.046
158
NTR005 Nutritional Deficiency Disease 33 0.046
159
TRC020 Tracheitis 33 0.046
160
P RNL066 Renal Tubular Acidosis, Distal, Ad 32 0.046
161
c ATM068 Autoimmune Hypoparathyroidism 30 0.046
162
c OST051 Osteopetrosis Autosomal Recessive 1 29 0.046
163
GRC002 Gracile Bone Dysplasia 28 0.046
164
c KNN004 Kenny-Caffey Syndrome Type 1 26 0.046
165
c ACT053 Acute Thyroiditis 24 0.046
166
JJN008 Jejunoileitis 23 0.046
167
c TBL012 Tubular Aggregate Myopathy 22 0.046
168
INT147 Intrauterine Growth Restriction, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 22 0.046
169
c BNG076 Benign Exophthalmos Syndrome 22 0.046
170
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 22 0.046
171
c PSD035 Pseudohypoparathyroidism Type 2 21 0.046
172
P OCL041 Oculomotor Apraxia Cogan Type 20 0.046
173
c CNG373 Congenital Generalized Lipodystrophy Type 3 20 0.046
174
OST008 Osteosclerotic Myeloma 18 0.046
175
XLN114 X-Linked Intellectual Disability - Craniofacioskeletal Syndrome 12 0.046
176
CSR002 Casr-Related Disorders 5 0.046