Search results for hypocalciuric hypercalcemia

64 hits were found for hypocalciuric hypercalcemia

# Family MCID Name MIFTS Score
1
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 33 13.921
2
c HYP314 Hypocalciuric Hypercalcemia, Type I 38 13.774
3
c HYP317 Hypocalciuric Hypercalcemia, Type Ii 36 13.015
4
P FML068 Familial Hypocalciuric Hypercalcemia 46 11.256
5
c HYP615 Hyperparathyroidism, Familial Primary 56 4.466
6
P HYP069 Hyperparathyroidism 58 0.524
7
P PNC044 Pancreatitis 61 0.223
8
P HYP237 Hypercalcemia, Infantile 47 0.212
9
ADN018 Adenoma 58 0.196
10
PRT029 Parathyroid Adenoma 48 0.188
11
P BRS047 Breast Cancer 100 0.177
12
P HYP024 Hypoparathyroidism 53 0.156
13
P CHN059 Chondrocalcinosis 41 0.152
14
MNR003 Mineral Metabolism Disease 38 0.146
15
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.136
16
ALR002 Al-Raqad Syndrome 36 0.136
17
P MLT074 Multiple Endocrine Neoplasia 56 0.134
18
NRN004 Neuroendocrine Tumor 56 0.129
19
HPT074 Hepatic Adenoma, Somatic 50 0.117
20
HNM002 Hinman Syndrome 25 0.117
21
INS001 Insulinoma 61 0.096
22
ALK013 Alkaptonuria 54 0.096
23
HYP068 Hyperostosis 40 0.096
24
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 36 0.096
25
ADP007 Adie Pupil 34 0.096
26
MTS004 Metastatic Insulinoma 19 0.096
27
HYP315 Hyperparathyroidism, Neonatal 35 0.091
28
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 16 0.085
29
P APL001 Aplastic Anemia 75 0.068
30
P PLM036 Pulmonary Fibrosis 71 0.068
31
P EPL164 Epilepsy 66 0.068
32
LNG099 Lung Disease 64 0.068
33
P DYS007 Dyskeratosis Congenita 63 0.068
34
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.068
35
INT066 Interstitial Lung Disease 59 0.068
36
P EPS003 Episodic Ataxia 57 0.068
37
MCN017 Meconium Ileus 54 0.068
38
CRH005 Crohn's Colitis 52 0.068
39
c EPS035 Episodic Ataxia, Type 2 51 0.068
40
c SPN309 Spinocerebellar Ataxia 6 51 0.068
41
NCT008 Nicotine Dependence, Protection Against 49 0.068
42
P KBK002 Kabuki Syndrome 1 49 0.068
43
LMB002 Lambert-Eaton Myasthenic Syndrome 49 0.068
44
c EPL100 Epilepsy, Generalized, with Febrile Seizures Plus, Type 5 47 0.068
45
P PTT014 Pitt-Hopkins Syndrome 47 0.068
46
EPS004 Episodic Ataxia/myokymia Syndrome 45 0.068
47
c SPN100 Spinocerebellar Ataxia 27 43 0.068
48
HYP099 Hyperferritinemia-Cataract Syndrome 42 0.068
49
EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 42 0.068
50
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 41 0.068
51
CRV045 Cervical Intraepithelial Neoplasia 38 0.068
52
c FNC042 Fanconi Anemia, Complementation Group D2 37 0.068
53
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 35 0.068
54
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.068
55
RNL021 Renal Tubular Transport Disease 32 0.068
56
c PLM044 Pulmonary Fibrosis, Familial 31 0.068
57
EPL072 Epilepsy, Nocturnal Frontal Lobe, 3 30 0.068
58
c DYS039 Dyskeratosis Congenita Autosomal Dominant 29 0.068
59
INH011 Inherited Bone Marrow Failure Syndromes 27 0.068
60
BCH003 Boucher-Neuhauser Syndrome 27 0.068
61
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 25 0.068
62
c EPS015 Episodic Ataxia, Type 7 23 0.068
63
MNG003 Mungan Syndrome 22 0.068
64
ATS327 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2 21 0.068
Content
Loading form....