Search results for hypomagnesemia

149 hits were found for hypomagnesemia

# Family MCID Name MIFTS Score
1
HYP550 Hypomagnesemia 1, Intestinal 38 11.246
2
c HYP534 Hypomagnesemia 3, Renal 37 8.499
3
P HYP210 Hypomagnesemia 2, Renal 33 8.330
4
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 7.476
5
GTL001 Gitelman Syndrome 62 6.603
6
PRM237 Primary Hypomagnesemia 40 6.134
7
c HYP302 Hypomagnesemia 4, Renal 18 5.884
8
c HYP445 Hypomagnesemia 6, Renal 19 5.092
9
HYP646 Hypomagnesemia, Seizures, and Mental Retardation 17 3.648
10
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 11 2.327
11
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 15 2.187
12
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 2.116
13
HYP800 Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial 4 2.116
14
P HYP733 Hypercalciuria, Absorptive, 2 37 0.304
15
NPH003 Nephrocalcinosis 49 0.300
16
HYP005 Hypokalemia 53 0.283
17
MNR003 Mineral Metabolism Disease 33 0.148
18
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.148
19
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 0.140
20
P HYP024 Hypoparathyroidism 55 0.140
21
P CHN059 Chondrocalcinosis 47 0.140
22
HPT082 Hepatic Adenomas, Familial 52 0.131
23
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 45 0.131
24
HYP017 Hypophosphatemia 45 0.121
25
ALR002 Al-Raqad Syndrome 30 0.121
26
P ANR048 Aniridia 1 68 0.110
27
HYP025 Hyperphosphatemia 48 0.110
28
ANR038 Anorexia Nervosa 1 21 0.110
29
BLD137 Blood Group--Ahonen 17 0.110
30
AGN016 Aging 65 0.099
31
RCK004 Rickets 63 0.099
32
P DRR001 Diarrhea 60 0.099
33
P HYP069 Hyperparathyroidism 58 0.099
34
NPH009 Nephrolithiasis 57 0.099
35
MNG003 Mungan Syndrome 34 0.099
36
P ORT004 Orthostatic Intolerance 68 0.085
37
P THY054 Thyrotoxic Periodic Paralysis 54 0.085
38
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 0.085
39
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.085
40
SLP010 Slipped Capital Femoral Epiphysis 37 0.085
41
c HYP563 Hyperpigmentation, Familial Progressive, 1 16 0.085
42
CNG034 Congestive Heart Failure 74 0.070
43
P KDN018 Kidney Disease 69 0.070
44
KRN002 Kearns-Sayre Syndrome 59 0.070
45
P MYP006 Myopia 56 0.070
46
P TRM003 Tremor 54 0.070
47
CRD223 Cardiac Arrhythmia 52 0.070
48
P SHR001 Short Bowel Syndrome 52 0.070
49
P RNL007 Renal Tubular Acidosis 51 0.070
50
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 51 0.070
51
P PSD015 Pseudohypoparathyroidism 50 0.070
52
HDN002 Head Injury 48 0.070
53
c BRT050 Bartter Syndrome, Type 2, Antenatal 43 0.070
54
ADP007 Adie Pupil 41 0.070
55
PRT019 Protein-Losing Enteropathy 40 0.070
56
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.070
57
BHR001 Behr Syndrome 36 0.070
58
CHL109 Childhood Apraxia of Speech 31 0.070
59
c BRT052 Bartter Syndrome, Type 1, Antenatal 29 0.070
60
CLC053 Colchicine Poisoning 24 0.070
61
BLD163 Blood Group, Dombrock System 23 0.070
62
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 13 0.070
63
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.070
64
P CLR023 Colorectal Cancer 98 0.049
65
P ART022 Arthritis 77 0.049
66
P MDL005 Medulloblastoma 76 0.049
67
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.049
68
ALP046 Alport Syndrome, X-Linked 74 0.049
69
P DBT009 Diabetes Mellitus 72 0.049
70
c CHR089 Chronic Kidney Failure 72 0.049
71
P ADN016 Adenocarcinoma 71 0.049
72
c BTT014 Beta-Thalassemia 70 0.049
73
P HYD006 Hydrocephalus 68 0.049
74
SRC014 Sarcoma 68 0.049
75
LNG099 Lung Disease 67 0.049
76
ISC004 Ischemia 66 0.049
77
GST050 Gastrointestinal System Disease 66 0.049
78
P CLC063 Celiac Disease 1 65 0.049
79
P THL005 Thalassemia 65 0.049
80
P INT068 Intestinal Disease 65 0.049
81
MDD011 Mood Disorder 64 0.049
82
LPT001 Leptospirosis 64 0.049
83
P PNC044 Pancreatitis 64 0.049
84
CRD119 Cardiac Arrest 63 0.049
85
HYP056 Hypoglycemia 62 0.049
86
c ACT027 Acute Pancreatitis 61 0.049
87
SDD001 Sudden Infant Death Syndrome 61 0.049
88
ETN001 Eating Disorder 61 0.049
89
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.049
90
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.049
91
SRC027 Sarcoma, Synovial 58 0.049
92
URN009 Urinary System Disease 58 0.049
93
P SJG008 Sjogren Syndrome 58 0.049
94
BRN106 Burns 57 0.049
95
P DNT020 Dent Disease 1 55 0.049
96
CLN019 Colonic Disease 55 0.049
97
STR020 Strabismus 55 0.049
98
SPS003 Spastic Diplegia 55 0.049
99
P HYP014 Hyperuricemia 54 0.049
100
P FNC004 Fanconi Syndrome 54 0.049
101
P PRM002 Primary Hyperoxaluria 53 0.049
102
CLN015 Colon Adenocarcinoma 53 0.049
103
P PTT014 Pitt-Hopkins Syndrome 52 0.049
104
RTN023 Retinitis 52 0.049
105
BRT005 Barth Syndrome 52 0.049
106
CLB010 Coloboma of Macula 52 0.049
107
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.049
108
CLD007 Cold Agglutinin Disease 50 0.049
109
PRT030 Parathyroid Gland Disease 50 0.049
110
RNL024 Renal Glucosuria 50 0.049
111
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.049
112
RNL011 Renal Osteodystrophy 49 0.049
113
INT303 Intracranial Hypertension, Idiopathic 49 0.049
114
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.049
115
AST006 Astigmatism 48 0.049
116
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.049
117
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.049
118
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.049
119
IDP073 Idiopathic Hypercalciuria 46 0.049
120
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.049
121
RNL051 Renal Cysts and Diabetes Syndrome 45 0.049
122
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.049
123
ACT167 Acute Generalized Exanthematous Pustulosis 42 0.049
124
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.049
125
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.049
126
CRN025 Corneal Dystrophy 42 0.049
127
JJN008 Jejunoileitis 41 0.049
128
CHR078 Chorioretinitis 41 0.049
129
BSL009 Basal Ganglia Calcification 39 0.049
130
RCT017 Rectal Disease 38 0.049
131
ALC010 Alcoholic Cardiomyopathy 38 0.049
132
P HRD086 Hereditary Hypophosphatemic Rickets 36 0.049
133
PYR004 Pyuria 34 0.049
134
CRT012 Cortical Blindness 34 0.049
135
c CHN022 Chondrocalcinosis 2 32 0.049
136
CYN002 Cyanosis, Transient Neonatal 32 0.049
137
CHR077 Chorioretinal Scar 32 0.049
138
MTL002 Metal Metabolism Disorder 30 0.049
139
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.049
140
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 29 0.049
141
VSL002 Visual Epilepsy 27 0.049
142
OSM001 Osmotic Diarrhea 27 0.049
143
IMP003 Impaired Renal Function Disease 25 0.049
144
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 24 0.049
145
HYP018 Hyperglobulinemic Purpura 23 0.049
146
INF043 Infantile Apnea 21 0.049
147
EPP010 Epiphysiolysis of the Hip 20 0.049
148
c BRT024 Bartter Syndrome Type 4 18 0.049
149
FXP001 Foxp2-Related Speech and Language Disorders 12 0.049
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