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 28 8.441
2
c HYP210 Hypomagnesemia 2, Renal 31 7.858
3
GTL001 Gitelman Syndrome 60 6.122
4
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 6.110
5
P HYP534 Hypomagnesemia 3, Renal 28 5.823
6
c HYP302 Hypomagnesemia 4, Renal 23 5.388
7
P PRM237 Primary Hypomagnesemia 28 4.918
8
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 17 4.751
9
c HYP445 Hypomagnesemia 6, Renal 22 4.586
10
HYP646 Hypomagnesemia, Seizures, and Mental Retardation 13 2.928
11
MYK003 Myokymia 1 with or Without Hypomagnesemia 9 2.880
12
c FML326 Familial Primary Hypomagnesemia 7 2.327
13
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 6 2.224
14
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 7 2.071
15
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 2.071
16
NPH003 Nephrocalcinosis 47 0.347
17
HYP005 Hypokalemia 52 0.284
18
MNR003 Mineral Metabolism Disease 39 0.186
19
HYP268 Hypercalciuria, Absorptive 31 0.170
20
ALR002 Al-Raqad Syndrome 36 0.152
21
P HYP024 Hypoparathyroidism 52 0.142
22
P DRR001 Diarrhea 60 0.142
23
P CRD011 Cardiomyopathy 66 0.131
24
HYP017 Hypophosphatemia 43 0.131
25
P HYP192 Hypocalcemia, Autosomal Dominant 50 0.120
26
P CHN059 Chondrocalcinosis 43 0.120
27
BHR001 Behr Syndrome 43 0.107
28
HYP025 Hyperphosphatemia 45 0.107
29
SSM001 Sesame Syndrome 53 0.093
30
P NPH009 Nephrolithiasis 59 0.093
31
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 56 0.076
32
KRN002 Kearns-Sayre Syndrome 60 0.076
33
CNG034 Congestive Heart Failure 72 0.076
34
P PTT014 Pitt-Hopkins Syndrome 51 0.076
35
CRH001 Crohn's Disease 76 0.076
36
P RCK004 Rickets 59 0.076
37
c SZR008 Seizures, Benign Neonatal, 1 32 0.076
38
NTR005 Nutritional Deficiency Disease 51 0.076
39
P BRT004 Bartter Disease 46 0.076
40
P MYP006 Myopia 58 0.076
41
DYS140 Dyskinesia, Familial, with Facial Myokymia 22 0.076
42
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 26 0.076
43
WHP001 Whipple Disease 49 0.076
44
P HYP069 Hyperparathyroidism 57 0.076
45
CYN002 Cyanosis, Transient Neonatal 29 0.076
46
MNG003 Mungan Syndrome 21 0.076
47
P SHR001 Short Bowel Syndrome 51 0.076
48
P TRM003 Tremor 54 0.076
49
CRH005 Crohn's Colitis 50 0.076
50
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.076
51
STT004 Steatorrhea 41 0.076
52
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 20 0.076
53
PRT019 Protein-Losing Enteropathy 42 0.076
54
CHR078 Chorioretinitis 41 0.076
55
VSL002 Visual Epilepsy 30 0.076
56
CLC007 Calcium Metabolism Disease 39 0.076
57
HDN002 Head Injury 47 0.076
58
c CLR082 Colorectal Cancer 7 22 0.076
59
CHR077 Chorioretinal Scar 30 0.076
60
FXP001 Foxp2-Related Speech and Language Disorders 15 0.076
61
OTP003 Oto-Palatal-Digital Syndrome 14 0.076
62
MRB004 Meier Blumberg Imahorn Syndrome 3 0.076
63
c SPS168 Spastic Paraplegia 56 13 0.076
64
P OBS005 Obesity 91 0.054
65
P MDL005 Medulloblastoma 76 0.054
66
BRT005 Barth Syndrome 53 0.054
67
P HYD006 Hydrocephalus 68 0.054
68
P KDN018 Kidney Disease 64 0.054
69
KRT002 Keratomalacia 50 0.054
70
CRD119 Cardiac Arrest 63 0.054
71
P URF003 Urofacial Syndrome 1 51 0.054
72
P SDD001 Sudden Infant Death Syndrome 60 0.054
73
c BRT034 Bartter Syndrome, Type 2 28 0.054
74
c BRT033 Bartter Syndrome, Type 1 29 0.054
75
P ART022 Arthritis 73 0.054
76
LPT001 Leptospirosis 65 0.054
77
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.054
78
c CHN022 Chondrocalcinosis 2 25 0.054
79
CHY002 Chylomicron Retention Disease 54 0.054
80
c CNG401 Congenital Heart Disease 67 0.054
81
c CHR089 Chronic Kidney Failure 67 0.054
82
URN009 Urinary System Disease 52 0.054
83
MTH009 Mouth Disease 63 0.054
84
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 34 0.054
85
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.054
86
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 25 0.054
87
P THL005 Thalassemia 61 0.054
88
HRT007 Heart Cancer 51 0.054
89
SRC014 Sarcoma 66 0.054
90
HYP056 Hypoglycemia 60 0.054
91
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 39 0.054
92
c PRM005 Primary Hyperparathyroidism 56 0.054
93
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.054
94
LNG099 Lung Disease 63 0.054
95
P PNC044 Pancreatitis 62 0.054
96
BSL009 Basal Ganglia Calcification 41 0.054
97
P THY054 Thyrotoxic Periodic Paralysis 46 0.054
98
PRT030 Parathyroid Gland Disease 49 0.054
99
P SPS003 Spastic Diplegia 49 0.054
100
MRC001 Marchiafava Bignami Disease 33 0.054
101
RNL011 Renal Osteodystrophy 48 0.054
102
c ACT027 Acute Pancreatitis 59 0.054
103
CRT012 Cortical Blindness 36 0.054
104
ACT167 Acute Generalized Exanthematous Pustulosis 39 0.054
105
ALC010 Alcoholic Cardiomyopathy 38 0.054
106
CRN025 Corneal Dystrophy 40 0.054
107
INF043 Infantile Apnea 17 0.054
108
P PSD015 Pseudohypoparathyroidism 43 0.054
109
P HRT017 Heart Tumor 34 0.054
110
JJN008 Jejunoileitis 38 0.054
111
c CNG216 Congenital Hydrocephalus 35 0.054
112
c ADL079 Adult Heart Tumor 17 0.054
113
IMP003 Impaired Renal Function Disease 36 0.054
114
BRN106 Burns 52 0.054
115
SLP010 Slipped Capital Femoral Epiphysis 32 0.054
116
VTM003 Vitamin Metabolic Disorder 31 0.054