Search results for hypomagnesemia

148 hits were found for hypomagnesemia

# Family MCID Name MIFTS Score
1
HYP550 Hypomagnesemia 1, Intestinal 39 10.864
2
c HYP210 Hypomagnesemia 2, Renal 33 8.550
3
P HYP534 Hypomagnesemia 3, Renal 29 7.496
4
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 7.178
5
PRM237 Primary Hypomagnesemia 42 7.082
6
GTL001 Gitelman Syndrome 61 6.253
7
c HYP302 Hypomagnesemia 4, Renal 24 5.896
8
c HYP445 Hypomagnesemia 6, Renal 25 5.120
9
HYP646 Hypomagnesemia, Seizures, and Mental Retardation 14 3.648
10
MYK003 Myokymia 1 with or Without Hypomagnesemia 10 2.948
11
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 6 2.224
12
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 7 2.116
13
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 2.116
14
NPH003 Nephrocalcinosis 48 0.301
15
HYP005 Hypokalemia 51 0.271
16
MNR003 Mineral Metabolism Disease 38 0.156
17
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.131
18
P HYP024 Hypoparathyroidism 53 0.131
19
HPT074 Hepatic Adenoma, Somatic 50 0.121
20
HYP017 Hypophosphatemia 43 0.121
21
HNM002 Hinman Syndrome 25 0.121
22
P CHN059 Chondrocalcinosis 41 0.111
23
HYP268 Hypercalciuria, Absorptive 35 0.111
24
P DRR001 Diarrhea 60 0.099
25
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.099
26
HYP025 Hyperphosphatemia 47 0.099
27
ALR002 Al-Raqad Syndrome 36 0.099
28
P CRD011 Cardiomyopathy 68 0.086
29
P NPH009 Nephrolithiasis 60 0.086
30
SSM001 Sesame Syndrome 52 0.086
31
CNG034 Congestive Heart Failure 72 0.070
32
P RCK004 Rickets 61 0.070
33
KRN002 Kearns-Sayre Syndrome 61 0.070
34
P HYP069 Hyperparathyroidism 58 0.070
35
P SHR001 Short Bowel Syndrome 49 0.070
36
P THY054 Thyrotoxic Periodic Paralysis 48 0.070
37
HDN002 Head Injury 45 0.070
38
BHR001 Behr Syndrome 42 0.070
39
PRT019 Protein-Losing Enteropathy 42 0.070
40
NTR005 Nutritional Deficiency Disease 36 0.070
41
ADP007 Adie Pupil 34 0.070
42
HYP611 Hypoparathyroidism, X-Linked 20 0.070
43
CLC053 Colchicine Poisoning 15 0.070
44
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 9 0.070
45
P CLR023 Colorectal Cancer 97 0.049
46
P OBS005 Obesity 92 0.049
47
P MDL005 Medulloblastoma 77 0.049
48
P ART022 Arthritis 75 0.049
49
P HRT032 Heart Disease 75 0.049
50
CRH001 Crohn's Disease 75 0.049
51
P KDN018 Kidney Disease 66 0.049
52
P HYD006 Hydrocephalus 66 0.049
53
c CHR089 Chronic Kidney Failure 66 0.049
54
SRC014 Sarcoma 66 0.049
55
P THL005 Thalassemia 64 0.049
56
LNG099 Lung Disease 64 0.049
57
LPT001 Leptospirosis 62 0.049
58
HYP056 Hypoglycemia 61 0.049
59
P SDD001 Sudden Infant Death Syndrome 61 0.049
60
CRD119 Cardiac Arrest 61 0.049
61
MTH009 Mouth Disease 61 0.049
62
MDD011 Mood Disorder 61 0.049
63
P PNC044 Pancreatitis 61 0.049
64
P GST049 Gastrointestinal System Cancer 60 0.049
65
P ORL007 Oral Cavity Cancer 59 0.049
66
P HRM001 Hermansky-Pudlak Syndrome 59 0.049
67
KND001 Kindler Syndrome 57 0.049
68
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 57 0.049
69
CHY002 Chylomicron Retention Disease 57 0.049
70
c ACT027 Acute Pancreatitis 57 0.049
71
ORL011 Oral Cancer 56 0.049
72
P MYP006 Myopia 56 0.049
73
c HYP615 Hyperparathyroidism, Familial Primary 56 0.049
74
P TRM003 Tremor 54 0.049
75
RCT018 Rectal Neoplasm 54 0.049
76
BRT005 Barth Syndrome 52 0.049
77
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.049
78
BRN106 Burns 52 0.049
79
KRT002 Keratomalacia 52 0.049
80
P SPS003 Spastic Diplegia 52 0.049
81
CRH005 Crohn's Colitis 52 0.049
82
c INF071 Inflammatory Bowel Disease 1 51 0.049
83
CLN019 Colonic Disease 51 0.049
84
c KNN009 Kenny-Caffey Syndrome, Type 1 50 0.049
85
URN009 Urinary System Disease 50 0.049
86
P URF003 Urofacial Syndrome 1 50 0.049
87
MSC072 Muscle Cancer 49 0.049
88
WHP001 Whipple Disease 49 0.049
89
PRT030 Parathyroid Gland Disease 47 0.049
90
INT253 Intestinal Benign Neoplasm 47 0.049
91
P PTT014 Pitt-Hopkins Syndrome 47 0.049
92
BRD001 Brody Myopathy 47 0.049
93
HRT007 Heart Cancer 46 0.049
94
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.049
95
c HRM006 Hermansky-Pudlak Syndrome 3 46 0.049
96
c BRT034 Bartter Syndrome, Type 2 46 0.049
97
P PSD015 Pseudohypoparathyroidism 46 0.049
98
RNL011 Renal Osteodystrophy 45 0.049
99
P SKN013 Skin Benign Neoplasm 43 0.049
100
BSL009 Basal Ganglia Calcification 43 0.049
101
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.049
102
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.049
103
CRN025 Corneal Dystrophy 42 0.049
104
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.049
105
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.049
106
IDP073 Idiopathic Hypercalciuria 41 0.049
107
STT004 Steatorrhea 40 0.049
108
c HRM008 Hermansky-Pudlak Syndrome 5 40 0.049
109
RCT017 Rectal Disease 40 0.049
110
CHR078 Chorioretinitis 40 0.049
111
CRP010 Corpus Callosum Agenesis 38 0.049
112
ALC010 Alcoholic Cardiomyopathy 38 0.049
113
JJN008 Jejunoileitis 38 0.049
114
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.049
115
c CNG216 Congenital Hydrocephalus 37 0.049
116
TTR016 Tetra-Amelia Syndrome 36 0.049
117
MTL002 Metal Metabolism Disorder 35 0.049
118
c HRM009 Hermansky-Pudlak Syndrome 6 35 0.049
119
CRT012 Cortical Blindness 35 0.049
120
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 34 0.049
121
MSC004 Muscle Tissue Disease 34 0.049
122
SLP010 Slipped Capital Femoral Epiphysis 34 0.049
123
IMP003 Impaired Renal Function Disease 34 0.049
124
c BRT033 Bartter Syndrome, Type 1 34 0.049
125
c CLR080 Colorectal Cancer 5 32 0.049
126
P HRT017 Heart Tumor 32 0.049
127
c SZR008 Seizures, Benign Neonatal, 1 32 0.049
128
VSL002 Visual Epilepsy 31 0.049
129
CHR077 Chorioretinal Scar 30 0.049
130
VTM003 Vitamin Metabolic Disorder 30 0.049
131
c CNG195 Congenital Disorder of Glycosylation, Type Id 30 0.049
132
c CLR079 Colorectal Cancer 2 29 0.049
133
CYN002 Cyanosis, Transient Neonatal 28 0.049
134
IMM002 Immature Cataract 27 0.049
135
c CHN022 Chondrocalcinosis 2 25 0.049
136
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 25 0.049
137
c PTT055 Patterned Macular Dystrophy 3 23 0.049
138
DYS140 Dyskinesia, Familial, with Facial Myokymia 23 0.049
139
P PTT054 Patterned Macular Dystrophy 22 0.049
140
MNG003 Mungan Syndrome 22 0.049
141
HRM016 Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis 22 0.049
142
FML076 Familial Juvenile Hyperuricaemic Nephropathy 22 0.049
143
INF043 Infantile Apnea 20 0.049
144
MCC011 Mucociliary Clearance Disorder 16 0.049
145
c ADL079 Adult Heart Tumor 16 0.049
146
AND005 Androgen Insensitivity Syndrome, Mild 16 0.049
147
CLR028 Ciliary Dyskinesia-Bronchiectasis 15 0.049
148
MCR285 Microcephaly-Polymicrogyria-Corpus Callosum Agenesis Syndrome 9 0.049
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