Search results for "[genes] CASR"

41 hits were found for '[genes] CASR'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 46 21.497
2
HYP315 Hyperparathyroidism, Neonatal 33 21.497
3
P HYP069 Hyperparathyroidism 57 20.268
4
P HYP004 Hypercalcemia 54 20.268
5
c EPL142 Epilepsy Idiopathic Generalized 8 18 20.268
6
P CLR023 Colorectal Cancer 97 18.959
7
c PRM005 Primary Hyperparathyroidism 57 18.959
8
P NPH009 Nephrolithiasis 57 17.552
9
P PRT010 Parathyroid Carcinoma 59 16.023
10
HYP005 Hypokalemia 53 16.023
11
P HYP024 Hypoparathyroidism 51 16.023
12
c HYP314 Hypocalciuric Hypercalcemia, Type I 31 16.023
13
P OST002 Osteoporosis 80 14.332
14
P PNC044 Pancreatitis 60 14.332
15
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 53 14.332
16
URM002 Uremia 52 14.332
17
RNL011 Renal Osteodystrophy 49 14.332
18
P PRT029 Parathyroid Adenoma 48 14.332
19
P ATM019 Autoimmune Polyendocrine Syndrome 47 14.332
20
NPH003 Nephrocalcinosis 47 14.332
21
HYP025 Hyperphosphatemia 46 14.332
22
P FML068 Familial Hypocalciuric Hypercalcemia 33 14.332
23
c MLT136 Multiple Endocrine Neoplasia 1 68 12.411
24
GTL001 Gitelman Syndrome 62 12.411
25
PRT030 Parathyroid Gland Disease 50 12.411
26
P BRT004 Bartter Disease 49 12.411
27
OST004 Osteitis Fibrosa 45 12.411
28
CLC001 Calciphylaxis 43 12.411
29
MNR003 Mineral Metabolism Disease 43 12.411
30
SCN001 Secondary Hyperparathyroidism of Renal Origin 43 12.411
31
P CHN059 Chondrocalcinosis 43 12.411
32
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 46 10.134
33
SLL001 Sialolithiasis 43 10.134
34
CLC007 Calcium Metabolism Disease 43 10.134
35
PHS001 Phosphorus Metabolism Disease 43 10.134
36
c ATM068 Autoimmune Hypoparathyroidism 26 10.134
37
HYP268 Hypercalciuria, Absorptive 25 10.134
38
BRT041 Bartter Syndrome with Hypocalcemia 9 7.166
39
c CSR003 Casr-Related Familial Isolated Hypoparathyroidism 8 7.166
40
CSR001 Casr-Associated Familial Isolated Hypoparathyroidism 4 7.166
41
CSR002 Casr-Related Disorders 4 7.166