Search results for "hypomagnesemia"

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

112 hits were found for 'hypomagnesemia'

# Family MCID Name MIFTS Score
1
HYP550 Hypomagnesemia 1, Intestinal 28 8.446
2
c HYP210 Hypomagnesemia 2, Renal 32 7.829
3
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 26 6.406
4
GTL001 Gitelman Syndrome 60 6.113
5
P HYP534 Hypomagnesemia 3, Renal 29 5.802
6
c HYP302 Hypomagnesemia 4, Renal 25 5.376
7
P PRM237 Primary Hypomagnesemia 29 4.855
8
PRM201 Primary Hypomagnesemia with Secondary Hypocalcemia 14 4.722
9
c HYP445 Hypomagnesemia 6, Renal 23 4.573
10
c FML326 Familial Primary Hypomagnesemia 10 3.040
11
HYP646 Hypomagnesemia, Seizures, and Mental Retardation 13 2.930
12
MYK003 Myokymia 1 with or Without Hypomagnesemia 12 2.882
13
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 6 2.191
14
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 6 2.072
15
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 4 2.072
16
NPH003 Nephrocalcinosis 46 0.330
17
HYP005 Hypokalemia 51 0.287
18
P HYP024 Hypoparathyroidism 52 0.143
19
HYP017 Hypophosphatemia 42 0.133
20
MNR003 Mineral Metabolism Disease 41 0.133
21
P HYP192 Hypocalcemia, Autosomal Dominant 55 0.121
22
P CHN059 Chondrocalcinosis 45 0.121
23
HYP268 Hypercalciuria, Absorptive 37 0.121
24
P CRD011 Cardiomyopathy 67 0.108
25
P DRR001 Diarrhea 51 0.108
26
HYP025 Hyperphosphatemia 46 0.108
27
ALR002 Al-Raqad Syndrome 36 0.108
28
P NPH009 Nephrolithiasis 60 0.094
29
SSM001 Sesame Syndrome 53 0.094
30
CNG034 Congestive Heart Failure 71 0.077
31
KRN002 Kearns-Sayre Syndrome 59 0.077
32
P RCK004 Rickets 59 0.077
33
P HYP069 Hyperparathyroidism 57 0.077
34
P SHR001 Short Bowel Syndrome 48 0.077
35
HDN002 Head Injury 45 0.077
36
PRT019 Protein-Losing Enteropathy 41 0.077
37
NTR005 Nutritional Deficiency Disease 39 0.077
38
P OBS005 Obesity 93 0.054
39
P MDL005 Medulloblastoma 77 0.054
40
CRH001 Crohn's Disease 76 0.054
41
P HRT032 Heart Disease 76 0.054
42
P ART022 Arthritis 75 0.054
43
P HYD006 Hydrocephalus 67 0.054
44
c CHR089 Chronic Kidney Failure 66 0.054
45
SRC014 Sarcoma 66 0.054
46
MTH009 Mouth Disease 63 0.054
47
LPT001 Leptospirosis 63 0.054
48
CRD119 Cardiac Arrest 63 0.054
49
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.054
50
LNG099 Lung Disease 62 0.054
51
P SDD001 Sudden Infant Death Syndrome 61 0.054
52
P THL005 Thalassemia 61 0.054
53
HYP056 Hypoglycemia 61 0.054
54
P PNC044 Pancreatitis 60 0.054
55
P MYP006 Myopia 59 0.054
56
CHY002 Chylomicron Retention Disease 59 0.054
57
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.054
58
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 56 0.054
59
c ACT027 Acute Pancreatitis 56 0.054
60
c HYP615 Hyperparathyroidism, Familial Primary 55 0.054
61
KRT002 Keratomalacia 54 0.054
62
URN009 Urinary System Disease 53 0.054
63
BRT005 Barth Syndrome 53 0.054
64
P SPS003 Spastic Diplegia 53 0.054
65
CRH005 Crohn's Colitis 52 0.054
66
P URF003 Urofacial Syndrome 1 52 0.054
67
BRN106 Burns 52 0.054
68
P PTT014 Pitt-Hopkins Syndrome 51 0.054
69
MRC001 Marchiafava Bignami Disease 50 0.054
70
c ACT068 Acute Cystitis 50 0.054
71
HRT007 Heart Cancer 50 0.054
72
PRT030 Parathyroid Gland Disease 49 0.054
73
WHP001 Whipple Disease 48 0.054
74
P THY054 Thyrotoxic Periodic Paralysis 47 0.054
75
RNL011 Renal Osteodystrophy 47 0.054
76
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.054
77
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.054
78
P PSD015 Pseudohypoparathyroidism 44 0.054
79
BHR001 Behr Syndrome 44 0.054
80
BSL009 Basal Ganglia Calcification 43 0.054
81
CHR078 Chorioretinitis 41 0.054
82
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.054
83
c BRT034 Bartter Syndrome, Type 2 41 0.054
84
CRN025 Corneal Dystrophy 41 0.054
85
ACT167 Acute Generalized Exanthematous Pustulosis 40 0.054
86
STT004 Steatorrhea 40 0.054
87
ALC010 Alcoholic Cardiomyopathy 38 0.054
88
JJN008 Jejunoileitis 37 0.054
89
IMP003 Impaired Renal Function Disease 37 0.054
90
c CNG216 Congenital Hydrocephalus 36 0.054
91
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 36 0.054
92
CRT012 Cortical Blindness 36 0.054
93
P HRT017 Heart Tumor 35 0.054
94
SLP010 Slipped Capital Femoral Epiphysis 35 0.054
95
VTM003 Vitamin Metabolic Disorder 33 0.054
96
c BRT033 Bartter Syndrome, Type 1 33 0.054
97
c SZR008 Seizures, Benign Neonatal, 1 33 0.054
98
VSL002 Visual Epilepsy 32 0.054
99
CHR077 Chorioretinal Scar 30 0.054
100
c CHN022 Chondrocalcinosis 2 26 0.054
101
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 25 0.054
102
c CLR082 Colorectal Cancer 7 23 0.054
103
MNG003 Mungan Syndrome 22 0.054
104
DYS140 Dyskinesia, Familial, with Facial Myokymia 22 0.054
105
HYP611 Hypoparathyroidism, X-Linked 21 0.054
106
c ADL079 Adult Heart Tumor 19 0.054
107
INF043 Infantile Apnea 18 0.054
108
AND005 Androgen Insensitivity Syndrome, Mild 16 0.054
109
FXP001 Foxp2-Related Speech and Language Disorders 15 0.054
110
c SPS168 Spastic Paraplegia 56 13 0.054
111
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 9 0.054
112
MRB004 Meier Blumberg Imahorn Syndrome 3 0.054