Search results for "hypocalcemia"

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

169 hits were found for 'hypocalcemia'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 50 9.730
2
HYP550 Hypomagnesemia 1, Intestinal 22 4.245
3
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 14 4.126
4
c HYP564 Hypocalcemia, Autosomal Dominant 2 11 3.340
5
BRT041 Bartter Syndrome with Hypocalcemia 7 3.316
6
c KNN007 Kenny-Caffey Syndrome, Type 2 22 2.416
7
HYP025 Hyperphosphatemia 36 0.276
8
HYP024 Hypoparathyroidism 48 0.243
9
P HYP069 Hyperparathyroidism 57 0.178
10
P PSD015 Pseudohypoparathyroidism 47 0.145
11
HYP005 Hypokalemia 42 0.138
12
c PRM005 Primary Hyperparathyroidism 58 0.130
13
P RCK004 Rickets 58 0.122
14
GRV001 Graves' Disease 54 0.122
15
HYP017 Hypophosphatemia 42 0.122
16
P HYP004 Hypercalcemia 57 0.113
17
P CLC005 Celiac Disease 69 0.103
18
P OST001 Osteopetrosis 65 0.103
19
P VLC001 Velocardiofacial Syndrome 60 0.103
20
P DGR001 Digeorge Syndrome 49 0.103
21
P HYP599 Hypoparathyroidism, Familial Isolated 39 0.092
22
P FML068 Familial Hypocalciuric Hypercalcemia 37 0.092
23
P DLT002 Dilated Cardiomyopathy 77 0.080
24
CNG034 Congestive Heart Failure 69 0.080
25
P LKM002 Leukemia 66 0.080
26
P THY032 Thyroiditis 56 0.080
27
P HYP076 Hyperthyroidism 54 0.080
28
OST011 Osteomalacia 45 0.080
29
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.080
30
NTR005 Nutritional Deficiency Disease 28 0.080
31
P KNN002 Kenny-Caffey Syndrome 25 0.080
32
P MYC007 Myocardial Infarction 81 0.065
33
P SZR006 Seizure Disorder 56 0.065
34
P LYM026 Lymphoblastic Leukemia 55 0.065
35
ADN018 Adenoma 55 0.065
36
ACN002 Acanthosis Nigricans 55 0.065
37
P HPT021 Hepatitis 55 0.065
38
P MYL007 Myeloma 53 0.065
39
c PSD066 Pseudohypoparathyroidism, Type Ib 53 0.065
40
c ACT075 Acute Myocardial Infarction 57 0.065
41
P BRT004 Bartter Disease 51 0.065
42
P HYP065 Hyperaldosteronism 49 0.065
43
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 47 0.065
44
P PRT029 Parathyroid Adenoma 46 0.065
45
BSL009 Basal Ganglia Calcification 46 0.065
46
THR013 Thoracic Outlet Syndrome 45 0.065
47
P DRR001 Diarrhea 44 0.065
48
IMP004 Impetigo 43 0.065
49
BRN106 Burns 42 0.065
50
P TRC086 Trichohepatoenteric Syndrome 1 39 0.065
51
c OST137 Osteopetrosis, Autosomal Recessive 4 36 0.065
52
HNN001 Hennekam Syndrome 33 0.065
53
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 31 0.065
54
PRS063 Paresthesia 31 0.065
55
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 31 0.065
56
P ATX010 Ataxia Neuropathy Spectrum 29 0.065
57
RCK007 Rickets, Vitamin D-Resistant, Type Iia 27 0.065
58
c OST131 Osteopetrosis, Autosomal Dominant 2 27 0.065
59
P VTM008 Vitamin D-Dependent Rickets, Type I 27 0.065
60
c ALP060 Alpha Heavy-Chain Disease 26 0.065
61
WLD003 Waldmann Disease 24 0.065
62
THY001 Thyroid Crisis 21 0.065
63
c RNG005 Ring Chromosome 10 22 0.065
64
2P2001 2p21 Microdeletion Syndrome 18 0.065
65
FML229 Familial Cutaneous Collagenoma 17 0.065
66
IMP001 Impetigo Herpetiformis 16 0.065
67
DHL001 Dahlberg Borer Newcomer Syndrome 17 0.065
68
SCN043 Secondary Intestinal Lymphangiectasia 15 0.065
69
MLL017 Müllerian Derivatives - Lymphangiectasia - Polydactyly 13 0.065
70
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.065
71
P ALZ034 Alzheimer Disease 100 0.046
72
HPT023 Hepatocellular Carcinoma 95 0.046
73
P OST005 Osteogenesis Imperfecta 77 0.046
74
c MLT019 Multiple Myeloma 75 0.046
75
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.046
76
P LPR003 Leprosy 71 0.046
77
P OST002 Osteoporosis 71 0.046
78
ACR007 Acromegaly 69 0.046
79
P ANG001 Angelman Syndrome 66 0.046
80
P HLP001 Holoprosencephaly 65 0.046
81
P PNM007 Pneumonia 64 0.046
82
P THL005 Thalassemia 64 0.046
83
GTL001 Gitelman Syndrome 64 0.046
84
P CNG401 Congenital Heart Disease 62 0.046
85
c HYP595 Hypertension, Essential 66 0.046
86
P HYP086 Hypothyroidism 59 0.046
87
c MTB001 Metabolic Syndrome X 58 0.046
88
DRM006 Dermatitis 58 0.046
89
ACT049 Acute Disseminated Encephalomyelitis 57 0.046
90
P PRT010 Parathyroid Carcinoma 56 0.046
91
GST009 Gastroschisis 55 0.046
92
P PSR002 Psoriasis 54 0.046
93
P ESN007 Eosinophilia 54 0.046
94
PRP030 Purpura 54 0.046
95
CHR103 Charge Syndrome 54 0.046
96
DFC004 Deficiency Anemia 54 0.046
97
P PTT014 Pitt-Hopkins Syndrome 54 0.046
98
MYL020 Myelomeningocele 54 0.046
99
P MLT074 Multiple Endocrine Neoplasia 53 0.046
100
TYP007 Typhoid Fever 53 0.046
101
GTR002 Goiter 53 0.046
102
P MYP004 Myopathy 53 0.046
103
BRC012 Brucellosis 53 0.046
104
P HMR012 Hemorrhagic Fever 52 0.046
105
P PLY019 Polyneuropathy 52 0.046
106
P NPH009 Nephrolithiasis 51 0.046
107
TXC005 Toxic Shock Syndrome 51 0.046
108
ALP008 Alopecia 51 0.046
109
c HPT003 Hepatitis a 51 0.046
110
GLC003 Glucose Intolerance 50 0.046
111
P INT068 Intestinal Disease 50 0.046
112
NRN001 Neuroendocrine Carcinoma 50 0.046
113
THY033 Thyrotoxicosis 49 0.046
114
c SPN225 Spondyloarthropathy 1 48 0.046
115
c ACT073 Acute Leukemia 48 0.046
116
JHN001 Johanson-Blizzard Syndrome 48 0.046
117
CLC001 Calciphylaxis 47 0.046
118
P OPH004 Ophthalmoplegia 47 0.046
119
URM002 Uremia 47 0.046
120
PRT019 Protein-Losing Enteropathy 47 0.046
121
c PND001 Pain Disorder 46 0.046
122
RNL078 Renal Dysplasia 46 0.046
123
OST004 Osteitis Fibrosa 46 0.046
124
STT004 Steatorrhea 45 0.046
125
SPT005 Spotted Fever 45 0.046
126
P FNC004 Fanconi Syndrome 44 0.046
127
MDT001 Mediterranean Spotted Fever 43 0.046
128
INT075 Intracranial Hypertension 43 0.046
129
RNL011 Renal Osteodystrophy 43 0.046
130
LPR001 Lepromatous Leprosy 42 0.046
131
DNG002 Dengue Hemorrhagic Fever 50 0.046
132
TRN044 Transposition of the Great Arteries 41 0.046
133
NPH003 Nephrocalcinosis 41 0.046
134
P ACT150 Acute Adrenal Insufficiency 41 0.046
135
STP004 Staphylococcal Toxic Shock Syndrome 41 0.046
136
PLM010 Pulmonary Edema 41 0.046
137
PRN039 Paraneoplastic Syndromes 40 0.046
138
P CRN108 Cranioectodermal Dysplasia 1 40 0.046
139
P MLT008 Multinodular Goiter 40 0.046
140
IMG001 Image Syndrome 39 0.046
141
c OPT055 Optic Atrophy Plus Syndrome 40 0.046
142
MDS022 Mediastinitis 39 0.046
143
ETH004 Euthyroid Sick Syndrome 39 0.046
144
MCR018 Microcytic Anemia 39 0.046
145
MYC033 Myoclonus 39 0.046
146
FTL007 Fetal Hydantoin Syndrome 38 0.046
147
INT088 Intrinsic Factor Deficiency 38 0.046
148
SYN036 Syncope 37 0.046
149
P RNL066 Renal Tubular Acidosis, Distal, Ad 35 0.046
150
c HYP057 Hypervitaminosis D 35 0.046
151
P HYP265 Hypotonia 34 0.046
152
VSC018 Visceral Steatosis 33 0.046
153
c ART101 Aortic Valve Disease 2 32 0.046
154
TRC020 Tracheitis 27 0.046
155
c OST126 Osteopetrosis, Autosomal Recessive 1 27 0.046
156
GRC002 Gracile Bone Dysplasia 25 0.046
157
c KNN008 Kenny-Caffey Syndrome-1 21 0.046
158
OCL041 Oculomotor Apraxia Cogan Type 21 0.046
159
c ACT053 Acute Thyroiditis 20 0.046
160
JJN008 Jejunoileitis 20 0.046
161
c BNG076 Benign Exophthalmos Syndrome 19 0.046
162
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 16 0.046
163
c PSD035 Pseudohypoparathyroidism Type 2 16 0.046
164
CNG051 Congenital Alopecia X-Linked 15 0.046
165
OST008 Osteosclerotic Myeloma 15 0.046
166
PRS106 Persistence of Mullerian Derivatives with Lymphangiectasia and Postaxial Polydactyly 13 0.046
167
MNR003 Mineral Metabolism Disease 13 0.046
168
CRN156 Craniofacioskeletal Syndrome 10 0.046
169
CSR002 Casr-Related Disorders 4 0.046