Search results for "hypomagnesemia"

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

116 hits were found for 'hypomagnesemia'

# Family MCID Name MIFTS Score
1
HYP550 Hypomagnesemia 1, Intestinal 22 6.427
2
GTL001 Gitelman Syndrome 64 5.988
3
P HYP211 Hypomagnesemia Primary 13 5.290
4
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 14 4.926
5
c HYP621 Hypomagnesemia-2, Renal 18 4.465
6
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 17 4.447
7
ATS250 Autosomal Dominant Primary Hypomagnesemia with Hypocalciuria 12 4.447
8
c HYP302 Hypomagnesemia 4, Renal 12 4.428
9
c HYP445 Hypomagnesemia 6, Renal 11 4.407
10
c HYP509 Hypomagnesemia 6 10 3.969
11
FML291 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Without Severe Ocular Involvement 8 3.969
12
P HYP534 Hypomagnesemia 3, Renal 16 3.493
13
FML277 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis with Severe Ocular Involvement 16 3.424
14
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 2.806
15
MYK003 Myokymia 1 with or Without Hypomagnesemia 3 2.806
16
MNZ002 Manz Syndrome 7 2.005
17
NPH003 Nephrocalcinosis 41 0.325
18
HYP005 Hypokalemia 42 0.262
19
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.141
20
P NPH009 Nephrolithiasis 51 0.131
21
HYP024 Hypoparathyroidism 48 0.119
22
SCH016 Schimke Immunoosseous Dysplasia 46 0.119
23
P CHN059 Chondrocalcinosis 41 0.119
24
TTR016 Tetra-Amelia Syndrome 36 0.119
25
c MTB001 Metabolic Syndrome X 58 0.107
26
HYP017 Hypophosphatemia 42 0.107
27
NTR005 Nutritional Deficiency Disease 28 0.107
28
MNR003 Mineral Metabolism Disease 13 0.107
29
P PRM002 Primary Hyperoxaluria 68 0.093
30
P SZR006 Seizure Disorder 56 0.093
31
THR013 Thoracic Outlet Syndrome 45 0.093
32
P DRR001 Diarrhea 44 0.093
33
P MYP006 Myopia 41 0.093
34
P TRC086 Trichohepatoenteric Syndrome 1 39 0.093
35
HYP025 Hyperphosphatemia 36 0.093
36
HPT023 Hepatocellular Carcinoma 95 0.076
37
P RTN008 Retinitis Pigmentosa 72 0.076
38
P ANG001 Angelman Syndrome 66 0.076
39
c CHR089 Chronic Kidney Failure 57 0.076
40
P KDN018 Kidney Disease 57 0.076
41
ACN002 Acanthosis Nigricans 55 0.076
42
CLB001 Coloboma 54 0.076
43
KRN002 Kearns-Sayre Syndrome 52 0.076
44
P HYP192 Hypocalcemia, Autosomal Dominant 50 0.076
45
c SPN225 Spondyloarthropathy 1 48 0.076
46
PRT019 Protein-Losing Enteropathy 47 0.076
47
P SHR001 Short Bowel Syndrome 45 0.076
48
HDN002 Head Injury 41 0.076
49
c ART101 Aortic Valve Disease 2 32 0.076
50
P ATX010 Ataxia Neuropathy Spectrum 29 0.076
51
P OBS005 Obesity 94 0.053
52
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.053
53
P MDL005 Medulloblastoma 71 0.053
54
CNG034 Congestive Heart Failure 69 0.053
55
AND015 Androgen Insensitivity 69 0.053
56
CRH001 Crohn's Disease 71 0.053
57
P ART022 Arthritis 65 0.053
58
P THL005 Thalassemia 64 0.053
59
P SDD001 Sudden Infant Death Syndrome 62 0.053
60
SRC014 Sarcoma 61 0.053
61
P PNC044 Pancreatitis 59 0.053
62
P RCK004 Rickets 58 0.053
63
BRT005 Barth Syndrome 58 0.053
64
P HYP069 Hyperparathyroidism 57 0.053
65
c ACT027 Acute Pancreatitis 55 0.053
66
P PTT014 Pitt-Hopkins Syndrome 54 0.053
67
EYD002 Eye Disease 54 0.053
68
HYP056 Hypoglycemia 53 0.053
69
CLD007 Cold Agglutinin Disease 52 0.053
70
MYC002 Mycobacterium Avium Complex Disease 51 0.053
71
P BRT004 Bartter Disease 51 0.053
72
GLC003 Glucose Intolerance 50 0.053
73
P RTN025 Retinoschisis 50 0.053
74
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.053
75
RNL007 Renal Tubular Acidosis 48 0.053
76
P PSD015 Pseudohypoparathyroidism 47 0.053
77
P HYP014 Hyperuricemia 47 0.053
78
PSD002 Pseudotumor Cerebri 47 0.053
79
P SPR013 Spiradenoma 47 0.053
80
P BLN003 Blindness 47 0.053
81
P MNT147 Mental Retardation 46 0.053
82
c PND001 Pain Disorder 46 0.053
83
LPT001 Leptospirosis 46 0.053
84
BSL009 Basal Ganglia Calcification 46 0.053
85
STT004 Steatorrhea 45 0.053
86
RTN023 Retinitis 44 0.053
87
P STR020 Strabismus 44 0.053
88
OBS006 Obstructive Lung Disease 43 0.053
89
RNL011 Renal Osteodystrophy 43 0.053
90
BRN106 Burns 42 0.053
91
ALC010 Alcoholic Cardiomyopathy 41 0.053
92
CHR078 Chorioretinitis 40 0.053
93
ACT167 Acute Generalized Exanthematous Pustulosis 40 0.053
94
CRN025 Corneal Dystrophy 38 0.053
95
WHP001 Whipple Disease 37 0.053
96
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 37 0.053
97
CRT012 Cortical Blindness 36 0.053
98
AST006 Astigmatism 35 0.053
99
c CHN022 Chondrocalcinosis 2 28 0.053
100
c SZR008 Seizures, Benign Neonatal, 1 28 0.053
101
SSM001 Sesame Syndrome 27 0.053
102
c JVN024 Juvenile Hereditary Hemochromatosis 25 0.053
103
c BRT034 Bartter Syndrome, Type 2 24 0.053
104
c BRT033 Bartter Syndrome, Type 1 23 0.053
105
SLP010 Slipped Capital Femoral Epiphysis 23 0.053
106
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 22 0.053
107
c KNN008 Kenny-Caffey Syndrome-1 21 0.053
108
MNG003 Mungan Syndrome 21 0.053
109
JJN008 Jejunoileitis 20 0.053
110
INF043 Infantile Apnea 19 0.053
111
c BNG076 Benign Exophthalmos Syndrome 19 0.053
112
AND005 Androgen Insensitivity Syndrome, Mild 17 0.053
113
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 17 0.053
114
OTP003 Oto-Palatal-Digital Syndrome 14 0.053
115
P INT105 Intellectual Disability Multi-Gene Panels 15 0.053
116
MRB004 Meier Blumberg Imahorn Syndrome 3 0.053