Search results for "[genes] CASR"

42 hits were found for '[genes] CASR'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 49 21.414
2
P HYP004 Hypercalcemia 52 20.189
3
P HYP069 Hyperparathyroidism 50 20.189
4
HYP315 Hyperparathyroidism, Neonatal 39 20.189
5
c EPL142 Epilepsy Idiopathic Generalized 8 19 20.189
6
P CLR023 Colorectal Cancer 95 18.885
7
c PRM005 Primary Hyperparathyroidism 56 18.885
8
P NPH009 Nephrolithiasis 48 17.485
9
P PRT010 Parathyroid Carcinoma 53 15.961
10
P PNC044 Pancreatitis 51 15.961
11
P HYP024 Hypoparathyroidism 45 15.961
12
c HYP314 Hypocalciuric Hypercalcemia, Type I 28 15.961
13
P OST002 Osteoporosis 75 14.276
14
GTL001 Gitelman Syndrome 63 14.276
15
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 50 14.276
16
URM002 Uremia 44 14.276
17
OST011 Osteomalacia 42 14.276
18
P ATM019 Autoimmune Polyendocrine Syndrome 41 14.276
19
P PRT029 Parathyroid Adenoma 39 14.276
20
HYP005 Hypokalemia 39 14.276
21
RNL011 Renal Osteodystrophy 39 14.276
22
HYP025 Hyperphosphatemia 36 14.276
23
P FML068 Familial Hypocalciuric Hypercalcemia 31 14.276
24
P PRM002 Primary Hyperoxaluria 64 12.363
25
c MLT136 Multiple Endocrine Neoplasia 1 62 12.363
26
P BRT004 Bartter Disease 48 12.363
27
P CHN059 Chondrocalcinosis 38 12.363
28
CLC001 Calciphylaxis 37 12.363
29
OST004 Osteitis Fibrosa 37 12.363
30
PRT030 Parathyroid Gland Disease 35 12.363
31
SCN001 Secondary Hyperparathyroidism of Renal Origin 32 12.363
32
MNR003 Mineral Metabolism Disease 29 12.363
33
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 46 10.095
34
PHS001 Phosphorus Metabolism Disease 33 10.095
35
IDP073 Idiopathic Hypercalciuria 33 10.095
36
CLC007 Calcium Metabolism Disease 28 10.095
37
c ATM068 Autoimmune Hypoparathyroidism 23 10.095
38
HYP268 Hypercalciuria, Absorptive 21 10.095
39
BRT041 Bartter Syndrome with Hypocalcemia 7 7.138
40
c CSR003 Casr-Related Familial Isolated Hypoparathyroidism 7 7.138
41
CSR002 Casr-Related Disorders 5 7.138
42
CSR001 Casr-Associated Familial Isolated Hypoparathyroidism 4 7.138