Search results for hypocalciuric hypercalcemia

68 hits were found for hypocalciuric hypercalcemia

# Family MCID Name MIFTS Score
1
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 37 14.226
2
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 38 13.878
3
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 38 12.630
4
P FML068 Familial Hypocalciuric Hypercalcemia 49 11.981
5
c PRM005 Primary Hyperparathyroidism 59 4.922
6
P HYP726 Hypercalcemia, Infantile, 1 57 1.315
7
P HYP069 Hyperparathyroidism 58 0.520
8
P PNC044 Pancreatitis 64 0.214
9
PRT029 Parathyroid Adenoma 50 0.207
10
PRT010 Parathyroid Carcinoma 64 0.192
11
ADN018 Adenoma 63 0.189
12
P HYP024 Hypoparathyroidism 55 0.182
13
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 0.181
14
P BRS047 Breast Cancer 100 0.172
15
HYP776 Hyperparathyroidism, Neonatal Severe 39 0.166
16
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.156
17
P CHN059 Chondrocalcinosis 47 0.151
18
P ANR048 Aniridia 1 68 0.145
19
P MLT074 Multiple Endocrine Neoplasia 55 0.145
20
ANR038 Anorexia Nervosa 1 21 0.145
21
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.145
22
BLD137 Blood Group--Ahonen 17 0.145
23
NRN004 Neuroendocrine Tumor 58 0.144
24
PRT030 Parathyroid Gland Disease 50 0.144
25
P HYP733 Hypercalciuria, Absorptive, 2 37 0.143
26
MNR003 Mineral Metabolism Disease 33 0.141
27
ALR002 Al-Raqad Syndrome 30 0.141
28
HYP025 Hyperphosphatemia 48 0.134
29
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.124
30
HYP741 Hyperparathyroidism 2 with Jaw Tumors 49 0.116
31
RNL011 Renal Osteodystrophy 49 0.115
32
HPT082 Hepatic Adenomas, Familial 52 0.114
33
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 25 0.110
34
RCK004 Rickets 63 0.105
35
CLC001 Calciphylaxis 53 0.105
36
OST004 Osteitis Fibrosa 45 0.105
37
INS001 Insulinoma 66 0.100
38
PSD014 Pseudopseudohypoparathyroidism 56 0.100
39
ALK013 Alkaptonuria 56 0.100
40
HYP068 Hyperostosis 52 0.100
41
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.100
42
PHS001 Phosphorus Metabolism Disease 34 0.100
43
MTS004 Metastatic Insulinoma 14 0.100
44
c MLT160 Multiple Endocrine Neoplasia, Type Iia 65 0.087
45
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.081
46
OST011 Osteomalacia 52 0.081
47
c BLD140 Blood Group, I System 37 0.081
48
CRH001 Crohn's Disease 80 0.074
49
LNG099 Lung Disease 67 0.074
50
INT066 Interstitial Lung Disease 63 0.074
51
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.074
52
CRH005 Crohn's Colitis 53 0.074
53
P PTT014 Pitt-Hopkins Syndrome 52 0.074
54
BCH003 Boucher-Neuhauser Syndrome 29 0.074
55
BLD163 Blood Group, Dombrock System 23 0.074
56
P KBK002 Kabuki Syndrome 1 62 0.066
57
c PNC108 Pancreatitis, Hereditary 60 0.066
58
IMM158 Immune Suppression 57 0.066
59
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.066
60
ALC009 Alcoholic Liver Cirrhosis 53 0.066
61
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 50 0.066
62
IDP073 Idiopathic Hypercalciuria 46 0.066
63
HYP801 Hyperferritinemia with or Without Cataract 39 0.066
64
c CRN243 Carney Complex, Type 1 35 0.066
65
MGL033 Megalocornea-Mental Retardation Syndrome 28 0.066
66
IMP003 Impaired Renal Function Disease 25 0.066
67
MGL027 Megalocornea-Intellectual Disability Syndrome 22 0.066
68
P JVN024 Juvenile Hereditary Hemochromatosis 22 0.066
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