Search results for hypocalcemia

211 hits were found for hypocalcemia

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 58 12.667
2
HYP550 Hypomagnesemia 1, Intestinal 38 8.472
3
c HYP564 Hypocalcemia, Autosomal Dominant 2 25 6.685
4
c KNN007 Kenny-Caffey Syndrome, Type 2 29 4.387
5
P HYP024 Hypoparathyroidism 52 0.269
6
HYP025 Hyperphosphatemia 46 0.269
7
P HYP069 Hyperparathyroidism 56 0.165
8
P PSD015 Pseudohypoparathyroidism 46 0.153
9
HYP005 Hypokalemia 50 0.141
10
PRM237 Primary Hypomagnesemia 43 0.141
11
P HYP599 Hypoparathyroidism, Familial Isolated 36 0.141
12
P OST001 Osteopetrosis 63 0.120
13
P GRV001 Graves' Disease 57 0.120
14
P DGR001 Digeorge Syndrome 54 0.120
15
HYP017 Hypophosphatemia 42 0.120
16
P CLC005 Celiac Disease 69 0.113
17
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.113
18
P VLC001 Velocardiofacial Syndrome 64 0.104
19
P RCK004 Rickets 57 0.104
20
VTM003 Vitamin Metabolic Disorder 31 0.104
21
c PSD067 Pseudohypoparathyroidism Ia 54 0.095
22
THY030 Thyroid Gland Disease 49 0.095
23
RCK007 Rickets, Vitamin D-Resistant, Type Iia 38 0.095
24
P CRD011 Cardiomyopathy 67 0.085
25
P FML068 Familial Hypocalciuric Hypercalcemia 47 0.085
26
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 42 0.085
27
P VTM008 Vitamin D-Dependent Rickets, Type I 38 0.085
28
c PSD104 Pseudohypoparathyroidism, Type Ii 33 0.085
29
c DLT002 Dilated Cardiomyopathy 74 0.074
30
P LKM002 Leukemia 72 0.074
31
HYP056 Hypoglycemia 60 0.074
32
P THY032 Thyroiditis 53 0.074
33
P HYP076 Hyperthyroidism 53 0.074
34
PRT029 Parathyroid Adenoma 49 0.074
35
MTB004 Metabolic Acidosis 47 0.074
36
HYP347 Hypotonia-Cystinuria Syndrome 45 0.074
37
BSL009 Basal Ganglia Calcification 43 0.074
38
c OST131 Osteopetrosis, Autosomal Dominant 2 42 0.074
39
BNS002 Bone Structure Disease 36 0.074
40
PRS063 Paresthesia 36 0.074
41
c KNN009 Kenny-Caffey Syndrome, Type 1 31 0.074
42
c PSD058 Pseudohypoparathyroidism Ic 29 0.074
43
GRC002 Gracile Bone Dysplasia 26 0.074
44
P MYC007 Myocardial Infarction 77 0.060
45
CNG034 Congestive Heart Failure 70 0.060
46
P HPT021 Hepatitis 68 0.060
47
THY028 Thyroid Cancer 68 0.060
48
CHR103 Charge Syndrome 65 0.060
49
P EPL164 Epilepsy 65 0.060
50
P PSR002 Psoriasis 64 0.060
51
P PRT010 Parathyroid Carcinoma 61 0.060
52
P LYM026 Lymphoblastic Leukemia 60 0.060
53
c ACT075 Acute Myocardial Infarction 59 0.060
54
CRD119 Cardiac Arrest 59 0.060
55
ADN018 Adenoma 58 0.060
56
P AGM005 Agammaglobulinemia, X-Linked 1 56 0.060
57
PGT001 Paget's Disease of Bone 53 0.060
58
BRN106 Burns 52 0.060
59
P HYP065 Hyperaldosteronism 50 0.060
60
P CRN108 Cranioectodermal Dysplasia 1 50 0.060
61
URM002 Uremia 48 0.060
62
LYM116 Lymph Node Disease 47 0.060
63
JHN001 Johanson-Blizzard Syndrome 47 0.060
64
PRT030 Parathyroid Gland Disease 47 0.060
65
c HYP726 Hypercalcemia, Infantile, 1 47 0.060
66
OST011 Osteomalacia 47 0.060
67
NPH003 Nephrocalcinosis 47 0.060
68
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.060
69
RNL011 Renal Osteodystrophy 44 0.060
70
HPT074 Hepatic Adenoma, Somatic 44 0.060
71
BRT030 Birth Defects 44 0.060
72
IMP004 Impetigo 42 0.060
73
OST004 Osteitis Fibrosa 39 0.060
74
BHR001 Behr Syndrome 38 0.060
75
c ATS282 Autosomal Recessive Malignant Osteopetrosis 38 0.060
76
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.060
77
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 36 0.060
78
PRT019 Protein-Losing Enteropathy 36 0.060
79
c ATM068 Autoimmune Hypoparathyroidism 33 0.060
80
THY001 Thyroid Crisis 27 0.060
81
HNM002 Hinman Syndrome 27 0.060
82
P RNL066 Renal Tubular Acidosis, Distal, Ad 26 0.060
83
P LYM124 Lymphangiectasia, Intestinal 26 0.060
84
IMP001 Impetigo Herpetiformis 25 0.060
85
c RNG005 Ring Chromosome 10 25 0.060
86
c ALP087 Alpha-Heavy Chain Disease 25 0.060
87
c MYP088 Myopathy, Tubular Aggregate, 2 22 0.060
88
ACR079 Acrodysostosis with Multiple Hormone Resistance 22 0.060
89
CLC053 Colchicine Poisoning 21 0.060
90
MLL022 Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly 20 0.060
91
LYM123 Lymphedema-Hypoparathyroidism Syndrome 19 0.060
92
CRN156 Craniofacioskeletal Syndrome 16 0.060
93
c SCN043 Secondary Intestinal Lymphangiectasia 15 0.060
94
CHR181 Chromosome 10p Deletion 10 0.060
95
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 7 0.060
96
P MLT019 Multiple Myeloma 82 0.043
97
c MLT136 Multiple Endocrine Neoplasia 1 68 0.043
98
P OST005 Osteogenesis Imperfecta 68 0.043
99
P MYP004 Myopathy 68 0.043
100
P PNM007 Pneumonia 66 0.043
101
ACR007 Acromegaly 66 0.043
102
P HLP001 Holoprosencephaly 65 0.043
103
P LPR003 Leprosy 63 0.043
104
P OST002 Osteoporosis 63 0.043
105
P THL005 Thalassemia 61 0.043
106
BRC012 Brucellosis 61 0.043
107
BLM001 Bloom Syndrome 61 0.043
108
TYP007 Typhoid Fever 61 0.043
109
GTL001 Gitelman Syndrome 61 0.043
110
c ACT073 Acute Leukemia 61 0.043
111
DFC004 Deficiency Anemia 60 0.043
112
P HYP086 Hypothyroidism 60 0.043
113
DNG002 Dengue Hemorrhagic Fever 60 0.043
114
P INT068 Intestinal Disease 59 0.043
115
P DRR001 Diarrhea 59 0.043
116
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 0.043
117
P TMT001 Timothy Syndrome 58 0.043
118
IMG001 Image Syndrome 58 0.043
119
P INT063 Intellectual Disability 58 0.043
120
CRT002 Cartilage-Hair Hypoplasia 58 0.043
121
PRP030 Purpura 57 0.043
122
P INF032 Infertility 57 0.043
123
P ORL007 Oral Cavity Cancer 57 0.043
124
c PNC108 Pancreatitis, Hereditary 57 0.043
125
c HPT003 Hepatitis a 56 0.043
126
ORL011 Oral Cancer 56 0.043
127
P CHN012 Chondrosarcoma 55 0.043
128
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.043
129
TXC005 Toxic Shock Syndrome 55 0.043
130
PSD014 Pseudopseudohypoparathyroidism 55 0.043
131
P PLY019 Polyneuropathy 54 0.043
132
P MLT074 Multiple Endocrine Neoplasia 54 0.043
133
P SZR006 Seizure Disorder 54 0.043
134
c HYP615 Hyperparathyroidism, Familial Primary 53 0.043
135
THL018 Thalassemia Major 52 0.043
136
P HMR012 Hemorrhagic Fever 52 0.043
137
PLM010 Pulmonary Edema 52 0.043
138
GTR002 Goiter 52 0.043
139
P PTT014 Pitt-Hopkins Syndrome 51 0.043
140
RNL078 Renal Dysplasia 50 0.043
141
MYL020 Myelomeningocele 50 0.043
142
SPT005 Spotted Fever 49 0.043
143
LPR001 Lepromatous Leprosy 49 0.043
144
INT075 Intracranial Hypertension 48 0.043
145
P FNC004 Fanconi Syndrome 48 0.043
146
ALC009 Alcoholic Liver Cirrhosis 48 0.043
147
PPL002 Papillary Carcinoma 47 0.043
148
CLC001 Calciphylaxis 47 0.043
149
ACT049 Acute Disseminated Encephalomyelitis 47 0.043
150
TRN044 Transposition of the Great Arteries 46 0.043
151
P ACT150 Acute Adrenal Insufficiency 46 0.043
152
P CHN059 Chondrocalcinosis 44 0.043
153
SYN036 Syncope 44 0.043
154
MCR018 Microcytic Anemia 44 0.043
155
OST003 Osteonecrosis 43 0.043
156
LYM020 Lymph Node Cancer 42 0.043
157
STP004 Staphylococcal Toxic Shock Syndrome 42 0.043
158
IDP073 Idiopathic Hypercalciuria 42 0.043
159
VSC018 Visceral Steatosis 41 0.043
160
MLT008 Multinodular Goiter 41 0.043
161
PHS001 Phosphorus Metabolism Disease 40 0.043
162
SCH003 Schizophreniform Disorder 40 0.043
163
c CHR579 Chiari Malformation Type Ii 40 0.043
164
GST071 Gastrointestinal Carcinoma 40 0.043
165
GST009 Gastroschisis 40 0.043
166
MDS022 Mediastinitis 40 0.043
167
STT004 Steatorrhea 40 0.043
168
c HYP317 Hypocalciuric Hypercalcemia, Type Ii 39 0.043
169
P HYP265 Hypotonia 39 0.043
170
c HYP314 Hypocalciuric Hypercalcemia, Type I 39 0.043
171
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 38 0.043
172
c HYP725 Hypocalciuric Hypercalcemia, Type Iii 38 0.043
173
OST115 Osteonecrosis of the Jaw 38 0.043
174
P HYP057 Hypervitaminosis D 38 0.043
175
HYP315 Hyperparathyroidism, Neonatal 37 0.043
176
ETH004 Euthyroid Sick Syndrome 36 0.043
177
INT088 Intrinsic Factor Deficiency 36 0.043
178
c OST129 Osteopetrosis, Autosomal Recessive 2 36 0.043
179
P PST059 Pustular Psoriasis 36 0.043
180
OST008 Osteosclerotic Myeloma 35 0.043
181
MDS018 Mediastinal Cancer 35 0.043
182
ADP007 Adie Pupil 35 0.043
183
JJN008 Jejunoileitis 34 0.043
184
FTL007 Fetal Hydantoin Syndrome 34 0.043
185
P ANX007 Anauxetic Dysplasia 1 34 0.043
186
P DYS023 Dyschromatosis Universalis Hereditaria 32 0.043
187
OST069 Osteopetrosis, Autosomal Recessive 3, with Renal Tubular Acidosis 32 0.043
188
PRN039 Paraneoplastic Syndromes 31 0.043
189
TRC020 Tracheitis 30 0.043
190
SCN001 Secondary Hyperparathyroidism of Renal Origin 30 0.043
191
c ACT053 Acute Thyroiditis 30 0.043
192
ALR002 Al-Raqad Syndrome 29 0.043
193
P HYP534 Hypomagnesemia 3, Renal 29 0.043
194
c OST134 Osteopetrosis, Autosomal Recessive 6 28 0.043
195
c OST125 Osteopetrosis, Autosomal Dominant 1 28 0.043
196
c PRM158 Primary Intestinal Lymphangiectasia 28 0.043
197
c CNG194 Congenital Disorder of Glycosylation, Type Ig 27 0.043
198
c OST136 Osteopetrosis, Autosomal Recessive 7 26 0.043
199
c OST120 Osteopetrosis, Autosomal Recessive 5 25 0.043
200
c LPD020 Lipodystrophy, Congenital Generalized, Type 3 25 0.043
201
c OST137 Osteopetrosis, Autosomal Recessive 4 24 0.043
202
P KNN002 Kenny-Caffey Syndrome 23 0.043
203
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 21 0.043
204
c BRT049 Bartter Syndrome, Type 5, Antenatal, Transient 20 0.043
205
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 17 0.043
206
BNM008 Bone Mineral Density, Low 17 0.043
207
AND005 Androgen Insensitivity Syndrome, Mild 16 0.043
208
THY021 Thyroid Malformation 13 0.043
209
TBL024 Tubular Renal Disease-Cardiomyopathy Syndrome 12 0.043
210
c FML196 Familial Isolated Hypoparathyroidism Due to Agenesis of Parathyroid Gland 11 0.043
211
CSR002 Casr-Related Disorders 3 0.043
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