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

115 hits were found for 'hypomagnesemia'

# ++ Fam MCID Name MIFTS Score
1
HYP210 Hypomagnesemia 2, Renal 15 5.322
2
GTL001 Gitelman Syndrome 54 5.133
3
HYP550 Hypomagnesemia 1, Intestinal 12 5.016
4
P HYP211 Hypomagnesemia Primary 11 5.001
5
RNL087 Renal Hypomagnesemia 4 12 4.891
6
HYP534 Hypomagnesemia 3, Renal 11 4.083
7
HYP445 Hypomagnesemia 6, Renal 6 3.994
8
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 12 3.459
9
c HYP564 Hypocalcemia, Autosomal Dominant 2 8 3.114
10
c HYP132 Hypomagnesemia with Secondary Hypocalcemia 11 2.913
11
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 3 2.824
12
c MYK003 Myokymia 1 with or Without Hypomagnesemia 2 2.824
13
HYP256 Hypomagnesemia, Renal, with Ocular Involvement 1 2.824
14
P HYP541 Hypotrichosis Simplex of Scalp 1 13 2.174
15
MNZ002 Manz Syndrome 10 2.153
16
NPH003 Nephrocalcinosis 52 0.295
17
HYP005 Hypokalemia 50 0.270
18
c ERL004 Early Yaws 29 0.187
19
P MYP018 Myopia 6 23 0.187
20
HYP540 Hypertension, Diastolic 19 0.187
21
ANK002 Ankylosing Spondylitis 75 0.171
22
CHL109 Childhood Apraxia of Speech 19 0.171
23
CNR017 Cone-Rod Dystrophy 9 19 0.171
24
THR013 Thoracic Outlet Syndrome 53 0.162
25
P NPH009 Nephrolithiasis 57 0.153
26
RHY001 Rhyns Syndrome 45 0.153
27
HPT023 Hepatocellular Carcinoma 69 0.132
28
P MYK002 Myokymia 40 0.132
29
MRB004 Meier Blumberg Imahorn Syndrome 3 0.132
30
P HYP024 Hypoparathyroidism 57 0.121
31
c DRR001 Diarrhea 49 0.121
32
c BRT034 Bartter Syndrome, Type 2 34 0.121
33
c CLB010 Coloboma of Macula 9 0.121
34
ACN002 Acanthosis Nigricans 70 0.108
35
HYP017 Hypophosphatemia 52 0.108
36
CNR004 Cone-Rod Dystrophy 2 47 0.108
37
WST001 West Syndrome 64 0.093
38
P MTR005 Mitral Valve Prolapse 54 0.093
39
HYP025 Hyperphosphatemia 48 0.093
40
CHR078 Chorioretinitis 41 0.093
41
SCH016 Schimke Immunoosseous Dysplasia 40 0.093
42
TTR016 Tetra-Amelia Syndrome 36 0.093
43
JVN024 Juvenile Hereditary Hemochromatosis 28 0.093
44
MNG003 Mungan Syndrome 15 0.093
45
CRH001 Crohn's Disease 78 0.076
46
P RFS001 Refsum Disease 73 0.076
47
BRN024 Bronchitis 71 0.076
48
P MYS003 Myasthenia Gravis 71 0.076
49
P ANG001 Angelman Syndrome 67 0.076
50
ART019 Aortic Valve Stenosis 64 0.076
51
c PRM002 Primary Hyperoxaluria 63 0.076
52
GLC003 Glucose Intolerance 62 0.076
53
NSY001 N Syndrome 57 0.076
54
CLB001 Coloboma 56 0.076
55
MYC002 Mycobacterium Avium Complex Disease 56 0.076
56
P SHR029 Short Syndrome 55 0.076
57
KRN002 Kearns-Sayre Syndrome 53 0.076
58
SHR001 Short Bowel Syndrome 53 0.076
59
ADL002 Adult Syndrome 50 0.076
60
STT004 Steatorrhea 49 0.076
61
P LCT002 Lactose Intolerance 49 0.076
62
HDN002 Head Injury 49 0.076
63
P THR090 Thrombocythemia 1 48 0.076
64
RTN025 Retinoschisis 47 0.076
65
CNR002 Cone-Rod Dystrophy 46 0.076
66
CHY002 Chylomicron Retention Disease 46 0.076
67
PRT019 Protein-Losing Enteropathy 46 0.076
68
PSD010 Pseudogout 40 0.076
69
c ATX010 Ataxia Neuropathy Spectrum 33 0.076
70
SYS006 Say Syndrome 29 0.076
71
NNS006 Non-Suppurative Otitis Media 24 0.076
72
P AMY001 Amyotrophic Lateral Sclerosis 87 0.054
73
P RTN008 Retinitis Pigmentosa 76 0.054
74
P ART022 Arthritis 75 0.054
75
P LBR001 Leber Congenital Amaurosis 74 0.054
76
CNG034 Congestive Heart Failure 74 0.054
77
THL005 Thalassemia 69 0.054
78
BTT002 Beta Thalassemia 69 0.054
79
c DBT009 Diabetes Mellitus 68 0.054
80
P MDL005 Medulloblastoma 66 0.054
81
P RCK004 Rickets 65 0.054
82
P SDD001 Sudden Infant Death Syndrome 65 0.054
83
P INS005 Insulin Resistance 62 0.054
84
PSY004 Psychotic Disorder 62 0.054
85
c HYP069 Hyperparathyroidism 57 0.054
86
BRT005 Barth Syndrome 54 0.054
87
SRC014 Sarcoma 54 0.054
88
c BLN003 Blindness 54 0.054
89
RTN023 Retinitis 53 0.054
90
P DNT039 Dent's Disease 52 0.054
91
CLD007 Cold Agglutinin Disease 52 0.054
92
c MNT147 Mental Retardation 51 0.054
93
LPT001 Leptospirosis 50 0.054
94
LPC002 Lip Cancer 50 0.054
95
RNL011 Renal Osteodystrophy 50 0.054
96
OBS006 Obstructive Lung Disease 49 0.054
97
P PTT014 Pitt-Hopkins Syndrome 49 0.054
98
c PSD015 Pseudohypoparathyroidism 49 0.054
99
P BRT004 Bartter Disease 48 0.054
100
WHP001 Whipple Disease 47 0.054
101
SYN006 Synovial Sarcoma 47 0.054
102
P HYP192 Hypocalcemia, Autosomal Dominant 45 0.054
103
CRT012 Cortical Blindness 44 0.054
104
ALC010 Alcoholic Cardiomyopathy 44 0.054
105
PSD002 Pseudotumor Cerebri 43 0.054
106
CRN025 Corneal Dystrophy 40 0.054
107
c MYP006 Myopia 36 0.054
108
P SLP004 Salpingo-Oophoritis 30 0.054
109
P CHN022 Chondrocalcinosis 2 25 0.054
110
SLP010 Slipped Capital Femoral Epiphysis 21 0.054
111
c HYP329 Hypoparathyroidism, Autosomal Dominant 21 0.054
112
AND005 Androgen Insensitivity Syndrome, Mild 19 0.054
113
c BNG076 Benign Exophthalmos Syndrome 17 0.054
114
INF043 Infantile Apnea 15 0.054
115
OTP003 Oto-Palatal-Digital Syndrome 13 0.054