Search results for "hypomagnesemia"

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

111 hits were found for 'hypomagnesemia'

# Family MCID Name MIFTS Score
1
GTL001 Gitelman Syndrome 73 6.520
2
P HYP210 Hypomagnesemia 2, Renal 24 5.807
3
HYP550 Hypomagnesemia 1, Intestinal 22 5.110
4
c RNL087 Renal Hypomagnesemia 4 20 4.990
5
P HYP211 Hypomagnesemia Primary 13 4.990
6
c HYP534 Hypomagnesemia 3, Renal 22 4.619
7
c HYP445 Hypomagnesemia 6, Renal 13 4.057
8
HYP132 Hypomagnesemia with Secondary Hypocalcemia 22 3.800
9
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 22 3.543
10
c HYP509 Hypomagnesemia 6 6 2.903
11
c HYP256 Hypomagnesemia, Renal, with Ocular Involvement 7 2.869
12
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 6 2.869
13
MYK003 Myokymia 1 with or Without Hypomagnesemia 4 2.869
14
MNZ002 Manz Syndrome 8 2.074
15
NPH003 Nephrocalcinosis 48 0.309
16
HYP005 Hypokalemia 49 0.262
17
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.154
18
P HYP024 Hypoparathyroidism 57 0.122
19
P MTB001 Metabolic Syndrome X 69 0.109
20
P NPH009 Nephrolithiasis 59 0.109
21
HYP017 Hypophosphatemia 48 0.109
22
NTR005 Nutritional Deficiency Disease 33 0.109
23
MNR003 Mineral Metabolism Disease 14 0.109
24
P MTR005 Mitral Valve Prolapse 59 0.095
25
c DRR001 Diarrhea 51 0.095
26
SCH016 Schimke Immunoosseous Dysplasia 48 0.095
27
TTR016 Tetra-Amelia Syndrome 43 0.095
28
HYP025 Hyperphosphatemia 43 0.095
29
SYN053 Syndromic Diarrhea 34 0.095
30
P LVR011 Liver Cancer 90 0.077
31
ANK002 Ankylosing Spondylitis 76 0.077
32
c PRM002 Primary Hyperoxaluria 73 0.077
33
P ANG001 Angelman Syndrome 71 0.077
34
KRN002 Kearns-Sayre Syndrome 63 0.077
35
ART019 Aortic Valve Stenosis 63 0.077
36
PRT019 Protein-Losing Enteropathy 55 0.077
37
THR013 Thoracic Outlet Syndrome 52 0.077
38
SHR001 Short Bowel Syndrome 51 0.077
39
HDN002 Head Injury 48 0.077
40
PSD010 Pseudogout 45 0.077
41
P BRT034 Bartter Syndrome, Type 2 43 0.077
42
P OBS005 Obesity 89 0.055
43
P RTN008 Retinitis Pigmentosa 86 0.055
44
c BTT002 Beta Thalassemia 82 0.055
45
P MDL005 Medulloblastoma 80 0.055
46
CNG034 Congestive Heart Failure 77 0.055
47
CRH001 Crohn's Disease 75 0.055
48
P ART022 Arthritis 74 0.055
49
c DBT009 Diabetes Mellitus 73 0.055
50
c THL005 Thalassemia 71 0.055
51
P SDD001 Sudden Infant Death Syndrome 71 0.055
52
SRC014 Sarcoma 68 0.055
53
CLB001 Coloboma 68 0.055
54
P RCK004 Rickets 67 0.055
55
BRT005 Barth Syndrome 66 0.055
56
c AMY001 Amyotrophic Lateral Sclerosis 66 0.055
57
P INS005 Insulin Resistance 64 0.055
58
ACN002 Acanthosis Nigricans 64 0.055
59
c HYP069 Hyperparathyroidism 64 0.055
60
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.055
61
GLC003 Glucose Intolerance 61 0.055
62
P RTN025 Retinoschisis 60 0.055
63
P PTT014 Pitt-Hopkins Syndrome 59 0.055
64
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.055
65
CLD007 Cold Agglutinin Disease 59 0.055
66
P DNT039 Dent's Disease 59 0.055
67
EYD002 Eye Disease 58 0.055
68
MYC002 Mycobacterium Avium Complex Disease 58 0.055
69
PSD002 Pseudotumor Cerebri 56 0.055
70
c MNT147 Mental Retardation 56 0.055
71
P SPR013 Spiradenoma 55 0.055
72
c PSD015 Pseudohypoparathyroidism 54 0.055
73
P HYP192 Hypocalcemia, Autosomal Dominant 54 0.055
74
c BRT004 Bartter Disease 53 0.055
75
RHY001 Rhyns Syndrome 53 0.055
76
LPT001 Leptospirosis 53 0.055
77
STT004 Steatorrhea 53 0.055
78
RTN023 Retinitis 53 0.055
79
BLN003 Blindness 52 0.055
80
CRN014 Cronkhite-Canada Syndrome 52 0.055
81
OBS006 Obstructive Lung Disease 52 0.055
82
RNL011 Renal Osteodystrophy 51 0.055
83
MNN014 Mononeuritis 51 0.055
84
P SZR006 Seizure Disorder 50 0.055
85
SYN006 Synovial Sarcoma 50 0.055
86
BRN106 Burns 49 0.055
87
ALC010 Alcoholic Cardiomyopathy 49 0.055
88
P ATX010 Ataxia Neuropathy Spectrum 47 0.055
89
MYK002 Myokymia 46 0.055
90
CRN025 Corneal Dystrophy 45 0.055
91
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.055
92
CHR078 Chorioretinitis 44 0.055
93
CRT012 Cortical Blindness 43 0.055
94
WHP001 Whipple Disease 41 0.055
95
c MYP006 Myopia 41 0.055
96
P MYP018 Myopia 6 36 0.055
97
CHL109 Childhood Apraxia of Speech 33 0.055
98
P CHN022 Chondrocalcinosis 2 32 0.055
99
SSM001 Sesame Syndrome 30 0.055
100
SLP010 Slipped Capital Femoral Epiphysis 27 0.055
101
c KNN004 Kenny-Caffey Syndrome Type 1 26 0.055
102
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 24 0.055
103
JJN008 Jejunoileitis 23 0.055
104
MNG003 Mungan Syndrome 22 0.055
105
c BNG076 Benign Exophthalmos Syndrome 22 0.055
106
AND005 Androgen Insensitivity Syndrome, Mild 21 0.055
107
c BRT033 Bartter Syndrome, Type 1 18 0.055
108
OTP003 Oto-Palatal-Digital Syndrome 17 0.055
109
INF043 Infantile Apnea 16 0.055
110
CLB010 Coloboma of Macula 15 0.055
111
MRB004 Meier Blumberg Imahorn Syndrome 3 0.055