Search results for "hypocalciuric hypercalcemia"

The MalaCard for "hypocalciuric hypercalcemia" has been retired.
Searching MalaCards for entries containing "hypocalciuric hypercalcemia"

280 hits were found for 'hypocalciuric hypercalcemia'

# Family MCID Name MIFTS Score
1
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 26 13.424
2
c HYP314 Hypocalciuric Hypercalcemia, Type I 33 13.267
3
c HYP317 Hypocalciuric Hypercalcemia, Type Ii 28 12.498
4
P FML068 Familial Hypocalciuric Hypercalcemia 38 10.352
5
c HYP615 Hyperparathyroidism, Familial Primary 55 4.394
6
P HYP069 Hyperparathyroidism 57 0.379
7
P PNC044 Pancreatitis 60 0.169
8
P HYP237 Hypercalcemia, Infantile 51 0.160
9
ADN018 Adenoma 59 0.145
10
PRT029 Parathyroid Adenoma 47 0.139
11
P BRS047 Breast Cancer 100 0.136
12
P HYP024 Hypoparathyroidism 52 0.118
13
P CHN059 Chondrocalcinosis 45 0.105
14
MNR003 Mineral Metabolism Disease 41 0.103
15
P MLT074 Multiple Endocrine Neoplasia 55 0.096
16
NRN004 Neuroendocrine Tumor 54 0.095
17
ALR002 Al-Raqad Syndrome 36 0.094
18
HPT074 Hepatic Adenoma, Somatic 51 0.082
19
HNM002 Hinman Syndrome 25 0.082
20
THR004 Thrombocytosis 55 0.076
21
P RHM011 Rheumatoid Arthritis 88 0.072
22
PRT036 Peritonitis 62 0.072
23
P PLY018 Polycythemia 57 0.072
24
HST011 Histoplasmosis 54 0.072
25
BRN106 Burns 52 0.072
26
PLM001 Pulmonary Tuberculosis 68 0.067
27
P PNM007 Pneumonia 66 0.067
28
P ESP024 Esophagitis 62 0.067
29
INS001 Insulinoma 59 0.067
30
ALK013 Alkaptonuria 55 0.067
31
HYP068 Hyperostosis 40 0.067
32
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 35 0.067
33
MTS004 Metastatic Insulinoma 19 0.067
34
SFT003 Soft Tissue Sarcoma 56 0.062
35
PRC002 Paracoccidioidomycosis 55 0.062
36
HDN004 Head and Neck Carcinoma 55 0.062
37
P MYC008 Myocarditis 54 0.062
38
MGK001 Megakaryocytic Leukemia 53 0.062
39
P ESS003 Essential Thrombocythemia 68 0.055
40
P MYL005 Myelofibrosis 67 0.055
41
LVR012 Liver Cirrhosis 67 0.055
42
HMT002 Hematologic Cancer 64 0.055
43
P LYM033 Lymphoproliferative Syndrome 53 0.055
44
END030 End Stage Renal Failure 52 0.055
45
P BLD051 Blood Coagulation Disease 45 0.055
46
IMM127 Immune System Cancer 42 0.055
47
GRN009 Granulomatous Hepatitis 38 0.055
48
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.047
49
CRH001 Crohn's Disease 76 0.047
50
MYL009 Myelodysplastic Syndrome 74 0.047
51
P APL001 Aplastic Anemia 73 0.047
52
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.047
53
P NRV007 Nervous System Disease 71 0.047
54
P DMN001 Diamond-Blackfan Anemia 68 0.047
55
P LPR003 Leprosy 68 0.047
56
P PLM036 Pulmonary Fibrosis 68 0.047
57
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.047
58
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.047
59
P MNN013 Meningitis 65 0.047
60
DFC004 Deficiency Anemia 65 0.047
61
P CNJ013 Conjunctivitis 65 0.047
62
BRC012 Brucellosis 65 0.047
63
P THR014 Thrombocytopenia 64 0.047
64
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.047
65
P DYS007 Dyskeratosis Congenita 63 0.047
66
PLY125 Polycythemia Vera, Somatic 63 0.047
67
RSP006 Respiratory System Disease 62 0.047
68
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.047
69
RCT015 Reactive Arthritis 62 0.047
70
LNG099 Lung Disease 62 0.047
71
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 62 0.047
72
DNG002 Dengue Hemorrhagic Fever 62 0.047
73
LSH001 Leishmaniasis 62 0.047
74
CNT047 Contact Dermatitis 62 0.047
75
APH001 Aphthous Stomatitis 62 0.047
76
CTN007 Cutaneous Leishmaniasis 62 0.047
77
CHG001 Chagas Disease 62 0.047
78
c ACT073 Acute Leukemia 62 0.047
79
TXC005 Toxic Shock Syndrome 61 0.047
80
HSH003 Hashimoto Thyroiditis 61 0.047
81
CHR063 Chronic Mucocutaneous Candidiasis 61 0.047
82
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.047
83
P INT068 Intestinal Disease 61 0.047
84
P ALP009 Alopecia Areata 61 0.047
85
TYP007 Typhoid Fever 61 0.047
86
c VRL010 Viral Hepatitis 61 0.047
87
BHC003 Behcet Syndrome 61 0.047
88
CNN005 Connective Tissue Disease 61 0.047
89
P TXP001 Toxoplasmosis 60 0.047
90
P SPN052 Spondyloarthropathy 60 0.047
91
TKY002 Takayasu Arteritis 60 0.047
92
GST045 Gastroenteritis 60 0.047
93
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.047
94
P LRY044 Larynx Cancer 59 0.047
95
P PRT013 Portal Hypertension 59 0.047
96
P UVT001 Uveitis 59 0.047
97
ALC006 Alcoholic Hepatitis 59 0.047
98
c HPT003 Hepatitis a 59 0.047
99
PRP030 Purpura 59 0.047
100
c SRC025 Sarcoidosis 1 58 0.047
101
INT066 Interstitial Lung Disease 58 0.047
102
SCH014 Schistosomiasis 58 0.047
103
BRN012 Bronchiolitis Obliterans 58 0.047
104
CRT002 Cartilage-Hair Hypoplasia 58 0.047
105
TNS005 Tonsillitis 58 0.047
106
ALP001 Alopecia Universalis 57 0.047
107
RHM027 Rheumatic Disease 57 0.047
108
ALL010 Allergic Contact Dermatitis 57 0.047
109
HMR004 Hemorrhagic Fever with Renal Syndrome 57 0.047
110
ERY003 Erythema Multiforme 57 0.047
111
IDP011 Idiopathic Interstitial Pneumonia 57 0.047
112
P EPS003 Episodic Ataxia 56 0.047
113
P RBL001 Rubella 56 0.047
114
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.047
115
JNT002 Joint Disorders 56 0.047
116
c SVR003 Severe Congenital Neutropenia 56 0.047
117
BRN002 Bronchiolitis 56 0.047
118
VSC003 Visceral Leishmaniasis 55 0.047
119
FLR002 Filariasis 55 0.047
120
CHR285 Chronic Myelomonocytic Leukemia 55 0.047
121
c EPS035 Episodic Ataxia, Type 2 55 0.047
122
P MNC007 Monocytic Leukemia 55 0.047
123
P LRY019 Laryngitis 55 0.047
124
P HMR012 Hemorrhagic Fever 55 0.047
125
LST001 Listeriosis 54 0.047
126
LYM027 Lymphopenia 54 0.047
127
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.047
128
c HPT007 Hepatitis E 54 0.047
129
FDL002 Food Allergy 54 0.047
130
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.047
131
P LCH002 Lichen Planus 53 0.047
132
P ACT135 Acute Graft Versus Host Disease 53 0.047
133
ALL026 Allergic Hypersensitivity Disease 53 0.047
134
ECH003 Echinococcosis 53 0.047
135
SLC006 Silicosis 53 0.047
136
SZR001 Sezary's Disease 53 0.047
137
BNM001 Bone Marrow Cancer 52 0.047
138
KRT006 Keratoconjunctivitis 52 0.047
139
CRH005 Crohn's Colitis 52 0.047
140
P PNC001 Pancytopenia 52 0.047
141
NRT004 Neuritis 52 0.047
142
VGT001 Vogt-Koyanagi-Harada Disease 52 0.047
143
OCL020 Ocular Cicatricial Pemphigoid 52 0.047
144
c INT064 Intermediate Uveitis 52 0.047
145
TRY001 Trypanosomiasis 52 0.047
146
ALV002 Alveolar Echinococcosis 51 0.047
147
MCN007 Meconium Aspiration Syndrome 51 0.047
148
IRN001 Iron Deficiency Anemia 51 0.047
149
P PTT014 Pitt-Hopkins Syndrome 51 0.047
150
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.047
151
c SPN309 Spinocerebellar Ataxia 6 51 0.047
152
MYC002 Mycobacterium Avium Complex Disease 51 0.047
153
P PNM006 Pneumoconiosis 51 0.047
154
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 51 0.047
155
RHM028 Rheumatic Heart Disease 51 0.047
156
c CHR417 Chronic Graft Versus Host Disease 50 0.047
157
PNN001 Panniculitis 50 0.047
158
NTR040 Neutropenia, Cyclic 50 0.047
159
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 50 0.047
160
IMM136 Immune System Disease 50 0.047
161
PRN021 Paranasal Sinus Disease 50 0.047
162
CYT005 Cytomegalovirus Retinitis 49 0.047
163
CCC002 Coccidiosis 49 0.047
164
P KBK002 Kabuki Syndrome 1 49 0.047
165
P SCL015 Scleritis 49 0.047
166
ESN005 Eosinophilic Gastroenteritis 49 0.047
167
HMG002 Hemoglobinuria 49 0.047
168
P PNV001 Panuveitis 49 0.047
169
c ANT034 Anterior Uveitis 49 0.047
170
P CHL066 Cholangitis 49 0.047
171
ALC009 Alcoholic Liver Cirrhosis 48 0.047
172
HYP063 Hypersplenism 48 0.047
173
MCR088 Microscopic Polyangiitis 48 0.047
174
LMB002 Lambert-Eaton Myasthenic Syndrome 48 0.047
175
P PLM006 Pulmonary Alveolar Proteinosis 48 0.047
176
P SCL009 Sclerosing Cholangitis 47 0.047
177
c EPL100 Epilepsy, Generalized, with Febrile Seizures Plus, Type 5 47 0.047
178
LKC003 Leukocyte Disease 47 0.047
179
MCR191 Microscopic Colitis 47 0.047
180
CNT046 Central Nervous System Vasculitis 47 0.047
181
MYL004 Myelodysplastic Myeloproliferative Cancer 47 0.047
182
BNN003 Bone Inflammation Disease 46 0.047
183
THR042 Thrombocytopenia, X-Linked 46 0.047
184
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 46 0.047
185
EPS004 Episodic Ataxia/myokymia Syndrome 46 0.047
186
ORL012 Oral Leukoplakia 46 0.047
187
PRR002 Pure Red-Cell Aplasia 46 0.047
188
BLD053 Blood Platelet Disease 46 0.047
189
HMN032 Human Herpesvirus 8 46 0.047
190
MCC002 Mucocutaneous Leishmaniasis 46 0.047
191
ELS001 Eales Disease 46 0.047
192
RFR010 Refractory Anemia 45 0.047
193
FLT011 Felty Syndrome 45 0.047
194
NTR018 Neutrophilia, Hereditary 45 0.047
195
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 0.047
196
EWN002 Ewing's Family of Tumors 45 0.047
197
STR072 Stromal Keratitis 45 0.047
198
IDP064 Idiopathic Neutropenia 45 0.047
199
PRS036 Parasitic Protozoa Infectious Disease 45 0.047
200
CLN003 Clonorchiasis 44 0.047
201
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 44 0.047
202
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.047
203
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.047
204
PLY020 Polyradiculoneuropathy 44 0.047
205
ACT200 Acute Monoblastic Leukemia 44 0.047
206
ANM001 Anemia of Prematurity 43 0.047
207
DNG001 Dengue Shock Syndrome 43 0.047
208
P PRL003 Proliferative Glomerulonephritis 43 0.047
209
P CPL003 Capillary Leak Syndrome 43 0.047
210
PRM025 Primary Bacterial Infectious Disease 43 0.047
211
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 42 0.047
212
c PRM225 Primary Thrombocytopenia 42 0.047
213
OPP002 Opportunistic Mycosis 42 0.047
214
P RSM001 Rasmussen Encephalitis 42 0.047
215
ESN004 Eosinophilic Gastritis 42 0.047
216
GRN017 Granulocytopenia 42 0.047
217
PRS012 Pars Planitis 42 0.047
218
HYP099 Hyperferritinemia-Cataract Syndrome 42 0.047
219
ASB001 Asbestosis 42 0.047
220
HYP458 Hyper Ige Syndrome 41 0.047
221
PTY001 Pityriasis Rosea 41 0.047
222
c CHR576 Chronic Beryllium Disease 41 0.047
223
PST053 Postherpetic Neuralgia 41 0.047
224
c ATM022 Autoimmune Myocarditis 41 0.047
225
NNT049 Nontuberculous Mycobacterial Lung Disease 41 0.047
226
LKP003 Leukoplakia 41 0.047
227
CRT004 Carotid Artery Thrombosis 41 0.047
228
c SPN100 Spinocerebellar Ataxia 27 41 0.047
229
ANC002 Anca-Associated Vasculitis 41 0.047
230
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 41 0.047
231
OLG015 Oligoarticular Juvenile Arthritis 40 0.047
232
NPH004 Nephropathia Epidemica 40 0.047
233
EXN001 Exanthema Subitum 40 0.047
234
DRG002 Drug-Induced Hepatitis 39 0.047
235
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.047
236
OLG001 Oligospermia 39 0.047
237
ATP013 Atopic Keratoconjunctivitis 39 0.047
238
EXT035 Extrinsic Cardiomyopathy 39 0.047
239
P BRY005 Beryllium Disease 38 0.047
240
SNL007 Senile Cataract 38 0.047
241
RVS001 Revesz Syndrome 38 0.047
242
CYC007 Cyclic Thrombocytopenia 37 0.047
243
ATM012 Autoimmune Disease of Blood 37 0.047
244
STC004 Stachybotrys Chartarum 37 0.047
245
IDP074 Idiopathic Bronchiectasis 37 0.047
246
ORF044 Orofacial Granulomatosis 36 0.047
247
LCH004 Lichen Disease 36 0.047
248
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 36 0.047
249
IRT001 Iritis 35 0.047
250
ECT004 Ecthyma 35 0.047
251
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 35 0.047
252
c MLT127 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 35 0.047
253
FLC001 Folic Acid Deficiency Anemia 34 0.047
254
c TYP024 Type Ii Mixed Cryoglobulinemia 34 0.047
255
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 33 0.047
256
TRN030 Transient Erythroblastopenia of Childhood 33 0.047
257
FSR001 Fusariosis 33 0.047
258
c ACT036 Acute Cholangitis 32 0.047
259
MYC022 Mycoplasmal Pneumonia 32 0.047
260
c DYS174 Dyskeratosis Congenita, Autosomal Dominant 6 31 0.047
261
NRW001 Norwegian Scabies 30 0.047
262
P RFR008 Refractory Anemia with Excess Blasts 30 0.047
263
CPL004 Caplan's Syndrome 30 0.047
264
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.047
265
c DYS039 Dyskeratosis Congenita Autosomal Dominant 29 0.047
266
TRC006 Trichosporonosis 28 0.047
267
ACT064 Acute Necrotizing Encephalitis 27 0.047
268
BCH003 Boucher-Neuhauser Syndrome 27 0.047
269
END018 Endometrium Carcinoma in Situ 26 0.047
270
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 25 0.047
271
INH011 Inherited Bone Marrow Failure Syndromes 25 0.047
272
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 23 0.047
273
VBR003 Vibrio Vulnificus Infection 23 0.047
274
c EPS015 Episodic Ataxia, Type 7 23 0.047
275
MNG003 Mungan Syndrome 22 0.047
276
c DYS040 Dyskeratosis Congenita Autosomal Recessive 21 0.047
277
FXP001 Foxp2-Related Speech and Language Disorders 15 0.047
278
TRC034 Torch Syndrome 14 0.047
279
c CNG418 Congenital Intrauterine Infection-Like Syndrome 14 0.047
280
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 12 0.047