Search results for "[genes] CASR"

41 hits were found for '[genes] CASR'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 43 21.497
2
HYP315 Hyperparathyroidism, Neonatal 30 21.497
3
P HYP069 Hyperparathyroidism 54 20.268
4
P HYP004 Hypercalcemia 49 20.268
5
c EPL142 Epilepsy Idiopathic Generalized 8 17 20.268
6
P CLR023 Colorectal Cancer 91 18.959
7
c PRM005 Primary Hyperparathyroidism 48 18.959
8
P NPH009 Nephrolithiasis 48 17.552
9
P PRT010 Parathyroid Carcinoma 55 16.023
10
P HYP024 Hypoparathyroidism 45 16.023
11
HYP005 Hypokalemia 44 16.023
12
c HYP314 Hypocalciuric Hypercalcemia, Type I 30 16.023
13
P OST002 Osteoporosis 76 14.332
14
P PNC044 Pancreatitis 53 14.332
15
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 50 14.332
16
URM002 Uremia 46 14.332
17
P ATM019 Autoimmune Polyendocrine Syndrome 42 14.332
18
P PRT029 Parathyroid Adenoma 41 14.332
19
RNL011 Renal Osteodystrophy 41 14.332
20
NPH003 Nephrocalcinosis 40 14.332
21
HYP025 Hyperphosphatemia 38 14.332
22
P FML068 Familial Hypocalciuric Hypercalcemia 32 14.332
23
c MLT136 Multiple Endocrine Neoplasia 1 61 12.411
24
GTL001 Gitelman Syndrome 57 12.411
25
P BRT004 Bartter Disease 51 12.411
26
PRT030 Parathyroid Gland Disease 40 12.411
27
OST004 Osteitis Fibrosa 38 12.411
28
CLC001 Calciphylaxis 37 12.411
29
P CHN059 Chondrocalcinosis 37 12.411
30
SCN001 Secondary Hyperparathyroidism of Renal Origin 33 12.411
31
MNR003 Mineral Metabolism Disease 33 12.411
32
SLL001 Sialolithiasis 41 10.134
33
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 36 10.134
34
PHS001 Phosphorus Metabolism Disease 35 10.134
35
CLC007 Calcium Metabolism Disease 32 10.134
36
HYP268 Hypercalciuria, Absorptive 20 10.134
37
c ATM068 Autoimmune Hypoparathyroidism 19 10.134
38
BRT041 Bartter Syndrome with Hypocalcemia 6 7.166
39
c CSR003 Casr-Related Familial Isolated Hypoparathyroidism 6 7.166
40
CSR001 Casr-Associated Familial Isolated Hypoparathyroidism 3 7.166
41
CSR002 Casr-Related Disorders 3 7.166