Search results for "[genes] CASR"

39 hits were found for '[genes] CASR'

# Family MCID Name MIFTS Score
1
P HYP192 Hypocalcemia, Autosomal Dominant 55 23.801
2
HYP315 Hyperparathyroidism, Neonatal 33 21.529
3
P HYP069 Hyperparathyroidism 57 20.297
4
c EPL142 Epilepsy Idiopathic Generalized 8 20 20.297
5
P CLR023 Colorectal Cancer 97 18.986
6
P NPH009 Nephrolithiasis 60 17.578
7
P PRT010 Parathyroid Carcinoma 62 16.046
8
P PNC044 Pancreatitis 60 16.046
9
P HYP024 Hypoparathyroidism 52 16.046
10
P FML068 Familial Hypocalciuric Hypercalcemia 38 16.046
11
c HYP314 Hypocalciuric Hypercalcemia, Type I 33 16.046
12
P OST002 Osteoporosis 64 14.352
13
GTL001 Gitelman Syndrome 60 14.352
14
c HYP615 Hyperparathyroidism, Familial Primary 55 14.352
15
HYP005 Hypokalemia 51 14.352
16
URM002 Uremia 50 14.352
17
OST011 Osteomalacia 48 14.352
18
PRT029 Parathyroid Adenoma 47 14.352
19
RNL011 Renal Osteodystrophy 47 14.352
20
HYP025 Hyperphosphatemia 46 14.352
21
P ATM019 Autoimmune Polyendocrine Syndrome 42 14.352
22
c MLT136 Multiple Endocrine Neoplasia 1 68 12.430
23
ATM033 Autoimmune Polyendocrinopathy Syndrome , Type I, with or Without Reversible Metaphyseal Dysplasia 51 12.430
24
PRT030 Parathyroid Gland Disease 49 12.430
25
P BRT004 Bartter Disease 46 12.430
26
P CHN059 Chondrocalcinosis 45 12.430
27
OST004 Osteitis Fibrosa 41 12.430
28
SCN001 Secondary Hyperparathyroidism of Renal Origin 41 12.430
29
MNR003 Mineral Metabolism Disease 41 12.430
30
CLC001 Calciphylaxis 40 12.430
31
HYP268 Hypercalciuria, Absorptive 37 12.430
32
P HYP237 Hypercalcemia, Infantile 51 10.149
33
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 44 10.149
34
PHS001 Phosphorus Metabolism Disease 42 10.149
35
IDP073 Idiopathic Hypercalciuria 40 10.149
36
c ATM068 Autoimmune Hypoparathyroidism 25 10.149
37
c CSR003 Casr-Related Familial Isolated Hypoparathyroidism 5 7.176
38
CSR001 Casr-Associated Familial Isolated Hypoparathyroidism 3 7.176
39
CSR002 Casr-Related Disorders 3 7.176