Search results for "hypomagnesemia"

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

106 hits were found for 'hypomagnesemia'

# Family MCID Name MIFTS Score
1
GTL001 Gitelman Syndrome 70 6.513
2
P HYP210 Hypomagnesemia 2, Renal 23 5.796
3
HYP550 Hypomagnesemia 1, Intestinal 20 5.101
4
P HYP211 Hypomagnesemia Primary 13 4.994
5
c RNL087 Renal Hypomagnesemia 4 18 4.973
6
c HYP534 Hypomagnesemia 3, Renal 19 4.605
7
c HYP445 Hypomagnesemia 6, Renal 13 4.060
8
HYP132 Hypomagnesemia with Secondary Hypocalcemia 22 3.807
9
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 21 3.516
10
c HYP509 Hypomagnesemia 6 6 2.906
11
c HYP256 Hypomagnesemia, Renal, with Ocular Involvement 7 2.871
12
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 6 2.871
13
MYK003 Myokymia 1 with or Without Hypomagnesemia 4 2.871
14
MNZ002 Manz Syndrome 8 2.076
15
NPH003 Nephrocalcinosis 49 0.314
16
HYP005 Hypokalemia 50 0.266
17
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.157
18
P HYP024 Hypoparathyroidism 57 0.124
19
P MTB001 Metabolic Syndrome X 70 0.111
20
P NPH009 Nephrolithiasis 58 0.111
21
HYP017 Hypophosphatemia 49 0.111
22
NTR005 Nutritional Deficiency Disease 33 0.111
23
MNR003 Mineral Metabolism Disease 14 0.111
24
P MTR005 Mitral Valve Prolapse 59 0.096
25
c DRR001 Diarrhea 52 0.096
26
SCH016 Schimke Immunoosseous Dysplasia 47 0.096
27
HYP025 Hyperphosphatemia 43 0.096
28
TTR016 Tetra-Amelia Syndrome 42 0.096
29
SYN053 Syndromic Diarrhea 34 0.096
30
P LVR011 Liver Cancer 91 0.078
31
ANK002 Ankylosing Spondylitis 77 0.078
32
c PRM002 Primary Hyperoxaluria 74 0.078
33
P ANG001 Angelman Syndrome 70 0.078
34
ART019 Aortic Valve Stenosis 64 0.078
35
KRN002 Kearns-Sayre Syndrome 63 0.078
36
THR013 Thoracic Outlet Syndrome 52 0.078
37
SHR001 Short Bowel Syndrome 52 0.078
38
PRT019 Protein-Losing Enteropathy 51 0.078
39
HDN002 Head Injury 49 0.078
40
PSD010 Pseudogout 46 0.078
41
P OBS005 Obesity 91 0.055
42
P RTN008 Retinitis Pigmentosa 86 0.055
43
P MDL005 Medulloblastoma 80 0.055
44
c BTT002 Beta Thalassemia 78 0.055
45
CNG034 Congestive Heart Failure 78 0.055
46
CRH001 Crohn's Disease 76 0.055
47
P ART022 Arthritis 75 0.055
48
c DBT009 Diabetes Mellitus 74 0.055
49
c THL005 Thalassemia 72 0.055
50
P SDD001 Sudden Infant Death Syndrome 71 0.055
51
SRC014 Sarcoma 70 0.055
52
P RCK004 Rickets 68 0.055
53
CLB001 Coloboma 68 0.055
54
c AMY001 Amyotrophic Lateral Sclerosis 67 0.055
55
P INS005 Insulin Resistance 65 0.055
56
BRT005 Barth Syndrome 65 0.055
57
c HYP069 Hyperparathyroidism 65 0.055
58
ACN002 Acanthosis Nigricans 63 0.055
59
GLC003 Glucose Intolerance 62 0.055
60
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.055
61
EYD002 Eye Disease 59 0.055
62
CLD007 Cold Agglutinin Disease 59 0.055
63
MYC002 Mycobacterium Avium Complex Disease 59 0.055
64
RTN025 Retinoschisis 59 0.055
65
P PTT014 Pitt-Hopkins Syndrome 59 0.055
66
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.055
67
P SPR013 Spiradenoma 56 0.055
68
P DNT039 Dent's Disease 56 0.055
69
PSD002 Pseudotumor Cerebri 55 0.055
70
c PSD015 Pseudohypoparathyroidism 55 0.055
71
c BRT004 Bartter Disease 54 0.055
72
LPT001 Leptospirosis 54 0.055
73
STT004 Steatorrhea 54 0.055
74
RTN023 Retinitis 54 0.055
75
BLN003 Blindness 53 0.055
76
OBS006 Obstructive Lung Disease 53 0.055
77
MNT147 Mental Retardation 52 0.055
78
CRN014 Cronkhite-Canada Syndrome 52 0.055
79
RNL011 Renal Osteodystrophy 51 0.055
80
RHY001 Rhyns Syndrome 51 0.055
81
MNN014 Mononeuritis 51 0.055
82
P SZR006 Seizure Disorder 51 0.055
83
BRN106 Burns 50 0.055
84
SYN006 Synovial Sarcoma 50 0.055
85
ALC010 Alcoholic Cardiomyopathy 49 0.055
86
MYK002 Myokymia 46 0.055
87
CRN025 Corneal Dystrophy 46 0.055
88
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.055
89
CHR078 Chorioretinitis 44 0.055
90
CRT012 Cortical Blindness 44 0.055
91
P ATX010 Ataxia Neuropathy Spectrum 43 0.055
92
c MYP006 Myopia 41 0.055
93
WHP001 Whipple Disease 41 0.055
94
P BRT034 Bartter Syndrome, Type 2 40 0.055
95
P MYP018 Myopia 6 36 0.055
96
P CHN022 Chondrocalcinosis 2 31 0.055
97
CHL109 Childhood Apraxia of Speech 31 0.055
98
SLP010 Slipped Capital Femoral Epiphysis 25 0.055
99
JJN008 Jejunoileitis 24 0.055
100
c BNG076 Benign Exophthalmos Syndrome 22 0.055
101
AND005 Androgen Insensitivity Syndrome, Mild 21 0.055
102
MNG003 Mungan Syndrome 19 0.055
103
OTP003 Oto-Palatal-Digital Syndrome 17 0.055
104
INF043 Infantile Apnea 16 0.055
105
CLB010 Coloboma of Macula 13 0.055
106
MRB004 Meier Blumberg Imahorn Syndrome 3 0.055