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
P HYP210 Hypomagnesemia 2, Renal 22 5.701
2
HYP550 Hypomagnesemia 1, Intestinal 20 5.046
3
GTL001 Gitelman Syndrome 67 5.002
4
HYP211 Hypomagnesemia Primary 12 4.969
5
c RNL087 Renal Hypomagnesemia 4 17 4.891
6
c HYP534 Hypomagnesemia 3, Renal 21 4.064
7
c HYP445 Hypomagnesemia 6, Renal 10 3.993
8
P HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 23 3.458
9
c HYP564 Hypocalcemia, Autosomal Dominant 2 14 3.402
10
HYP132 Hypomagnesemia with Secondary Hypocalcemia 13 2.888
11
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 6 2.824
12
c HYP256 Hypomagnesemia, Renal, with Ocular Involvement 4 2.824
13
MYK003 Myokymia 1 with or Without Hypomagnesemia 3 2.824
14
P HYP541 Hypotrichosis Simplex of Scalp 1 19 2.176
15
MNZ002 Manz Syndrome 6 1.997
16
NPH003 Nephrocalcinosis 53 0.299
17
HYP005 Hypokalemia 50 0.267
18
ERL004 Early Yaws 33 0.231
19
P MYP018 Myopia 6 29 0.189
20
HYP540 Hypertension, Diastolic 11 0.189
21
ANK002 Ankylosing Spondylitis 75 0.172
22
CHL109 Childhood Apraxia of Speech 24 0.172
23
CNR017 Cone-Rod Dystrophy 9 19 0.172
24
P NPH009 Nephrolithiasis 59 0.154
25
RHY001 Rhyns Syndrome 49 0.154
26
MNR003 Mineral Metabolism Disease 22 0.154
27
THR013 Thoracic Outlet Syndrome 54 0.134
28
MYK002 Myokymia 32 0.134
29
MRB004 Meier Blumberg Imahorn Syndrome 3 0.134
30
P HYP024 Hypoparathyroidism 58 0.122
31
P BRT034 Bartter Syndrome, Type 2 42 0.122
32
CLB010 Coloboma of Macula 13 0.122
33
HPT023 Hepatocellular Carcinoma 89 0.109
34
P MTB001 Metabolic Syndrome X 67 0.109
35
CNR004 Cone-Rod Dystrophy 2 53 0.109
36
HYP017 Hypophosphatemia 53 0.109
37
NTR005 Nutritional Deficiency Disease 28 0.109
38
WST001 West Syndrome 64 0.094
39
P MTR005 Mitral Valve Prolapse 55 0.094
40
c DRR001 Diarrhea 54 0.094
41
HYP025 Hyperphosphatemia 50 0.094
42
SCH016 Schimke Immunoosseous Dysplasia 49 0.094
43
CHR078 Chorioretinitis 45 0.094
44
TTR016 Tetra-Amelia Syndrome 43 0.094
45
SYN053 Syndromic Diarrhea 42 0.094
46
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.094
47
CRH001 Crohn's Disease 83 0.077
48
P RFS001 Refsum Disease 83 0.077
49
P MYS003 Myasthenia Gravis 79 0.077
50
BRN024 Bronchitis 76 0.077
51
ACN002 Acanthosis Nigricans 73 0.077
52
P ANG001 Angelman Syndrome 70 0.077
53
c PRM002 Primary Hyperoxaluria 68 0.077
54
ART019 Aortic Valve Stenosis 68 0.077
55
GLC003 Glucose Intolerance 63 0.077
56
CLB001 Coloboma 63 0.077
57
RTN025 Retinoschisis 60 0.077
58
KRN002 Kearns-Sayre Syndrome 59 0.077
59
CNR002 Cone-Rod Dystrophy 58 0.077
60
MYC002 Mycobacterium Avium Complex Disease 57 0.077
61
SHR001 Short Bowel Syndrome 55 0.077
62
P THR090 Thrombocythemia 1 54 0.077
63
ADL002 Adult Syndrome 52 0.077
64
P LCT002 Lactose Intolerance 50 0.077
65
STT004 Steatorrhea 50 0.077
66
CHY002 Chylomicron Retention Disease 49 0.077
67
PRT019 Protein-Losing Enteropathy 48 0.077
68
PSD010 Pseudogout 42 0.077
69
NNS006 Non-Suppurative Otitis Media 26 0.077
70
MNG003 Mungan Syndrome 18 0.077
71
P AMY001 Amyotrophic Lateral Sclerosis 100 0.055
72
P OBS005 Obesity 93 0.055
73
P LBR001 Leber Congenital Amaurosis 83 0.055
74
P MDL005 Medulloblastoma 82 0.055
75
CNG034 Congestive Heart Failure 81 0.055
76
P RTN008 Retinitis Pigmentosa 81 0.055
77
c DBT009 Diabetes Mellitus 80 0.055
78
P ART022 Arthritis 75 0.055
79
P SDD001 Sudden Infant Death Syndrome 70 0.055
80
c BTT002 Beta Thalassemia 70 0.055
81
PSY004 Psychotic Disorder 69 0.055
82
c THL005 Thalassemia 68 0.055
83
P RCK004 Rickets 67 0.055
84
BRN106 Burns 64 0.055
85
P DNT039 Dent's Disease 64 0.055
86
c HYP069 Hyperparathyroidism 63 0.055
87
SRC014 Sarcoma 63 0.055
88
BRT005 Barth Syndrome 62 0.055
89
RTN023 Retinitis 61 0.055
90
P PTT014 Pitt-Hopkins Syndrome 59 0.055
91
OBS006 Obstructive Lung Disease 57 0.055
92
RNL011 Renal Osteodystrophy 56 0.055
93
c PSD015 Pseudohypoparathyroidism 55 0.055
94
LPT001 Leptospirosis 55 0.055
95
LPC002 Lip Cancer 55 0.055
96
WHP001 Whipple Disease 53 0.055
97
SYN006 Synovial Sarcoma 51 0.055
98
c BRT004 Bartter Disease 49 0.055
99
ALC010 Alcoholic Cardiomyopathy 48 0.055
100
PSD002 Pseudotumor Cerebri 47 0.055
101
CLD007 Cold Agglutinin Disease 47 0.055
102
CRN025 Corneal Dystrophy 46 0.055
103
CRT012 Cortical Blindness 45 0.055
104
P ATX010 Ataxia Neuropathy Spectrum 44 0.055
105
c MYP006 Myopia 41 0.055
106
MNT147 Mental Retardation 35 0.055
107
P CHN022 Chondrocalcinosis 2 33 0.055
108
P SLP004 Salpingo-Oophoritis 31 0.055
109
c BNG076 Benign Exophthalmos Syndrome 21 0.055
110
AND005 Androgen Insensitivity Syndrome, Mild 18 0.055
111
OTP003 Oto-Palatal-Digital Syndrome 13 0.055