Search results for hypocalcemia

230 hits were found for hypocalcemia

# Family MCID Name MIFTS Score
1
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 13.455
2
HYP550 Hypomagnesemia 1, Intestinal 38 9.176
3
c HYP564 Hypocalcemia, Autosomal Dominant 2 19 5.656
4
c KNN007 Kenny-Caffey Syndrome, Type 2 30 4.376
5
P HYP024 Hypoparathyroidism 55 0.264
6
HYP025 Hyperphosphatemia 48 0.257
7
P HYP069 Hyperparathyroidism 58 0.159
8
P PSD015 Pseudohypoparathyroidism 50 0.148
9
HYP005 Hypokalemia 53 0.137
10
PRM237 Primary Hypomagnesemia 40 0.130
11
c PRM005 Primary Hyperparathyroidism 59 0.123
12
P HYP599 Hypoparathyroidism, Familial Isolated 39 0.123
13
P OST001 Osteopetrosis 70 0.116
14
P GRV001 Graves' Disease 62 0.116
15
DGR001 Digeorge Syndrome 55 0.116
16
HYP017 Hypophosphatemia 45 0.116
17
P CLC063 Celiac Disease 1 65 0.109
18
P HYP726 Hypercalcemia, Infantile, 1 57 0.109
19
VLC001 Velocardiofacial Syndrome 64 0.101
20
RCK004 Rickets 63 0.101
21
P HYP086 Hypothyroidism 62 0.101
22
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.101
23
THY030 Thyroid Gland Disease 51 0.092
24
VTM027 Vitamin D-Dependent Rickets, Type 2a 46 0.092
25
c PSD108 Pseudohypoparathyroidism, Type Ia 57 0.082
26
OST011 Osteomalacia 52 0.082
27
P FML068 Familial Hypocalciuric Hypercalcemia 49 0.082
28
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 42 0.082
29
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.082
30
BSL009 Basal Ganglia Calcification 39 0.082
31
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 37 0.082
32
c PSD104 Pseudohypoparathyroidism, Type Ii 34 0.082
33
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.082
34
MLL022 Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly 25 0.082
35
P DLT002 Dilated Cardiomyopathy 76 0.071
36
P LKM002 Leukemia 75 0.071
37
HYP056 Hypoglycemia 62 0.071
38
P HYP076 Hyperthyroidism 56 0.071
39
P THY032 Thyroiditis 56 0.071
40
PRT029 Parathyroid Adenoma 50 0.071
41
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.071
42
MTB004 Metabolic Acidosis 49 0.071
43
HYP347 Hypotonia-Cystinuria Syndrome 47 0.071
44
c OST131 Osteopetrosis, Autosomal Dominant 2 43 0.071
45
c PSD117 Pseudohypoparathyroidism, Type Ic 39 0.071
46
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.071
47
PRS063 Paresthesia 36 0.071
48
GRC002 Gracile Bone Dysplasia 25 0.071
49
P MYC007 Myocardial Infarction 81 0.058
50
P HPT021 Hepatitis 75 0.058
51
CNG034 Congestive Heart Failure 74 0.058
52
THY028 Thyroid Cancer 72 0.058
53
P EPL164 Epilepsy 70 0.058
54
P AGM019 Agammaglobulinemia, X-Linked 69 0.058
55
P ANR048 Aniridia 1 68 0.058
56
P LYM026 Lymphoblastic Leukemia 66 0.058
57
P PSR002 Psoriasis 65 0.058
58
AGN016 Aging 65 0.058
59
PRT010 Parathyroid Carcinoma 64 0.058
60
c ACT075 Acute Myocardial Infarction 64 0.058
61
ADN018 Adenoma 63 0.058
62
CRD119 Cardiac Arrest 63 0.058
63
PGT001 Paget's Disease of Bone 60 0.058
64
CHR103 Charge Syndrome 59 0.058
65
BRN106 Burns 57 0.058
66
P MYP006 Myopia 56 0.058
67
P MLT074 Multiple Endocrine Neoplasia 55 0.058
68
CLC001 Calciphylaxis 53 0.058
69
P CRN108 Cranioectodermal Dysplasia 1 53 0.058
70
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 52 0.058
71
URM002 Uremia 52 0.058
72
HPT082 Hepatic Adenomas, Familial 52 0.058
73
TMT001 Timothy Syndrome 52 0.058
74
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 51 0.058
75
HNN001 Hennekam Syndrome 50 0.058
76
PRT030 Parathyroid Gland Disease 50 0.058
77
RNL011 Renal Osteodystrophy 49 0.058
78
NPH003 Nephrocalcinosis 49 0.058
79
JHN001 Johanson-Blizzard Syndrome 48 0.058
80
PST011 Pustulosis of Palm and Sole 47 0.058
81
IMP004 Impetigo 45 0.058
82
OST004 Osteitis Fibrosa 45 0.058
83
PRT019 Protein-Losing Enteropathy 40 0.058
84
c ATS282 Autosomal Recessive Malignant Osteopetrosis 37 0.058
85
P HYP733 Hypercalciuria, Absorptive, 2 37 0.058
86
BHR001 Behr Syndrome 36 0.058
87
P LYM124 Lymphangiectasia, Intestinal 35 0.058
88
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 31 0.058
89
c ATM068 Autoimmune Hypoparathyroidism 30 0.058
90
THY001 Thyroid Crisis 30 0.058
91
IMP001 Impetigo Herpetiformis 29 0.058
92
c ALP087 Alpha-Heavy Chain Disease 27 0.058
93
c RNG005 Ring Chromosome 10 27 0.058
94
CLC053 Colchicine Poisoning 24 0.058
95
ACR079 Acrodysostosis with Multiple Hormone Resistance 24 0.058
96
c VSC053 Visceral Steatosis, Congenital 22 0.058
97
ANR038 Anorexia Nervosa 1 21 0.058
98
LYM123 Lymphedema-Hypoparathyroidism Syndrome 21 0.058
99
c MYP088 Myopathy, Tubular Aggregate, 2 21 0.058
100
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.058
101
CRN156 Craniofacioskeletal Syndrome 18 0.058
102
BLD137 Blood Group--Ahonen 17 0.058
103
c SCN043 Secondary Intestinal Lymphangiectasia 17 0.058
104
CHR181 Chromosome 10p Deletion 12 0.058
105
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 11 0.058
106
P ALZ034 Alzheimer Disease 95 0.041
107
MYL069 Myeloma, Multiple 86 0.041
108
P HRT032 Heart Disease 80 0.041
109
NRL016 Neural Tube Defects 79 0.041
110
P OST002 Osteoporosis 75 0.041
111
ALP046 Alport Syndrome, X-Linked 74 0.041
112
VNH007 Von Hippel-Lindau Syndrome 72 0.041
113
P DBT009 Diabetes Mellitus 72 0.041
114
BRC012 Brucellosis 71 0.041
115
P PNM007 Pneumonia 70 0.041
116
c MLT156 Multiple Endocrine Neoplasia, Type I 70 0.041
117
c BTT014 Beta-Thalassemia 70 0.041
118
ACR007 Acromegaly 70 0.041
119
P MYP004 Myopathy 69 0.041
120
P HLP001 Holoprosencephaly 67 0.041
121
BRT054 Brittle Bone Disorder 67 0.041
122
TYP007 Typhoid Fever 67 0.041
123
DNG002 Dengue Hemorrhagic Fever 66 0.041
124
P THL005 Thalassemia 65 0.041
125
P INT068 Intestinal Disease 65 0.041
126
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.041
127
c HPT003 Hepatitis a 63 0.041
128
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.041
129
OST003 Osteonecrosis 63 0.041
130
BLM001 Bloom Syndrome 62 0.041
131
DFC004 Deficiency Anemia 62 0.041
132
GTL001 Gitelman Syndrome 62 0.041
133
PRP030 Purpura 61 0.041
134
TXC005 Toxic Shock Syndrome 61 0.041
135
c ACT073 Acute Leukemia 61 0.041
136
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.041
137
P DRR001 Diarrhea 60 0.041
138
P HMR012 Hemorrhagic Fever 60 0.041
139
P INF032 Infertility 59 0.041
140
P LPR021 Leprosy 3 59 0.041
141
P PLY019 Polyneuropathy 58 0.041
142
CRT002 Cartilage-Hair Hypoplasia 58 0.041
143
PLM010 Pulmonary Edema 57 0.041
144
SPT005 Spotted Fever 57 0.041
145
P CHN012 Chondrosarcoma 56 0.041
146
PSD014 Pseudopseudohypoparathyroidism 56 0.041
147
GST009 Gastroschisis 55 0.041
148
DGN001 Degenerative Disc Disease 55 0.041
149
ALB001 Albright's Hereditary Osteodystrophy 55 0.041
150
P SZR006 Seizure Disorder 55 0.041
151
P FNC004 Fanconi Syndrome 54 0.041
152
MYL020 Myelomeningocele 54 0.041
153
GTR002 Goiter 53 0.041
154
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.041
155
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.041
156
LPR001 Lepromatous Leprosy 53 0.041
157
INT075 Intracranial Hypertension 53 0.041
158
P PTT014 Pitt-Hopkins Syndrome 52 0.041
159
P BRT004 Bartter Disease 52 0.041
160
ACT049 Acute Disseminated Encephalomyelitis 52 0.041
161
c GRV008 Graves Disease 1 52 0.041
162
P ACT150 Acute Adrenal Insufficiency 51 0.041
163
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.041
164
CHN070 Cohen-Gibson Syndrome 51 0.041
165
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 51 0.041
166
TRN044 Transposition of the Great Arteries 49 0.041
167
FBR009 Fibrous Dysplasia 49 0.041
168
RNL078 Renal Dysplasia 49 0.041
169
P MYP087 Myopathy, Tubular Aggregate, 1 48 0.041
170
c BRN108 Branchiootic Syndrome 1 47 0.041
171
P CHN059 Chondrocalcinosis 47 0.041
172
SYN036 Syncope 46 0.041
173
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 46 0.041
174
BNN003 Bone Inflammation Disease 46 0.041
175
IDP073 Idiopathic Hypercalciuria 46 0.041
176
STP004 Staphylococcal Toxic Shock Syndrome 45 0.041
177
MDS022 Mediastinitis 44 0.041
178
P MLT008 Multinodular Goiter 44 0.041
179
SCH003 Schizophreniform Disorder 44 0.041
180
c PSR021 Psoriasis 14, Pustular 44 0.041
181
c XNT010 Xanthinuria, Type I 43 0.041
182
MCR018 Microcytic Anemia 43 0.041
183
P GRW001 Growth Hormone Secreting Pituitary Adenoma 43 0.041
184
c CHR579 Chiari Malformation Type Ii 42 0.041
185
STT004 Steatorrhea 41 0.041
186
OST115 Osteonecrosis of the Jaw 41 0.041
187
c ALZ056 Alzheimer Disease 3 41 0.041
188
ADP007 Adie Pupil 41 0.041
189
JJN008 Jejunoileitis 41 0.041
190
c HYP057 Hypervitaminosis D 40 0.041
191
P HYP265 Hypotonia 40 0.041
192
P PST059 Pustular Psoriasis 40 0.041
193
ETH004 Euthyroid Sick Syndrome 40 0.041
194
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.041
195
HYP776 Hyperparathyroidism, Neonatal Severe 39 0.041
196
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.041
197
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.041
198
OST008 Osteosclerotic Myeloma 38 0.041
199
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 38 0.041
200
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 38 0.041
201
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.041
202
c BLD140 Blood Group, I System 37 0.041
203
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 37 0.041
204
c HYP534 Hypomagnesemia 3, Renal 37 0.041
205
P ANX007 Anauxetic Dysplasia 1 36 0.041
206
PRN039 Paraneoplastic Syndromes 35 0.041
207
INT088 Intrinsic Factor Deficiency 35 0.041
208
PHS001 Phosphorus Metabolism Disease 34 0.041
209
TRC020 Tracheitis 33 0.041
210
c OST129 Osteopetrosis, Autosomal Recessive 2 33 0.041
211
c OST163 Osteopetrosis, Autosomal Recessive 3 33 0.041
212
MNR003 Mineral Metabolism Disease 33 0.041
213
c PRM158 Primary Intestinal Lymphangiectasia 32 0.041
214
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.041
215
HRM003 Hormone Producing Pituitary Cancer 32 0.041
216
FTL007 Fetal Hydantoin Syndrome 31 0.041
217
c OST134 Osteopetrosis, Autosomal Recessive 6 31 0.041
218
ALR002 Al-Raqad Syndrome 30 0.041
219
c ACT053 Acute Thyroiditis 29 0.041
220
c CNG194 Congenital Disorder of Glycosylation, Type Ig 26 0.041
221
IST007 Isotretinoin Embryopathy-Like Syndrome 25 0.041
222
c OST136 Osteopetrosis, Autosomal Recessive 7 25 0.041
223
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 25 0.041
224
c OST125 Osteopetrosis, Autosomal Dominant 1 24 0.041
225
P KNN002 Kenny-Caffey Syndrome 24 0.041
226
c OST120 Osteopetrosis, Autosomal Recessive 5 23 0.041
227
c OST137 Osteopetrosis, Autosomal Recessive 4 23 0.041
228
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 17 0.041
229
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 13 0.041
230
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 12 0.041
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