Search results for "hypocalciuric hypercalcemia"

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

295 hits were found for 'hypocalciuric hypercalcemia'

# Family MCID Name MIFTS Score
1
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 26 12.130
2
c HYP314 Hypocalciuric Hypercalcemia, Type I 31 11.767
3
c HYP317 Hypocalciuric Hypercalcemia, Type Ii 26 11.133
4
P FML068 Familial Hypocalciuric Hypercalcemia 37 8.654
5
c PRM005 Primary Hyperparathyroidism 56 5.062
6
P HYP004 Hypercalcemia 54 0.995
7
P HYP069 Hyperparathyroidism 57 0.365
8
P PNC044 Pancreatitis 62 0.187
9
ADN018 Adenoma 59 0.152
10
PRT029 Parathyroid Adenoma 46 0.147
11
P BRS047 Breast Cancer 100 0.145
12
P CHN059 Chondrocalcinosis 43 0.143
13
MNR003 Mineral Metabolism Disease 39 0.138
14
ALR002 Al-Raqad Syndrome 36 0.135
15
P HYP024 Hypoparathyroidism 52 0.129
16
c ADL017 Adult T-Cell Leukemia 59 0.114
17
P MLT074 Multiple Endocrine Neoplasia 55 0.100
18
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.100
19
THR004 Thrombocytosis 55 0.095
20
P RHM011 Rheumatoid Arthritis 87 0.091
21
P ART022 Arthritis 73 0.091
22
HST011 Histoplasmosis 54 0.091
23
PRT036 Peritonitis 65 0.091
24
P GRV001 Graves' Disease 62 0.091
25
P PLY018 Polycythemia 58 0.091
26
BRN106 Burns 52 0.091
27
ALK013 Alkaptonuria 54 0.089
28
INS001 Insulinoma 60 0.089
29
LNG099 Lung Disease 63 0.089
30
HYP068 Hyperostosis 39 0.089
31
INT066 Interstitial Lung Disease 60 0.089
32
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 36 0.089
33
MTS004 Metastatic Insulinoma 18 0.089
34
P PNM007 Pneumonia 67 0.088
35
P ESP024 Esophagitis 62 0.088
36
PLM001 Pulmonary Tuberculosis 69 0.088
37
MLR002 Miliary Tuberculosis 39 0.088
38
PRC002 Paracoccidioidomycosis 57 0.084
39
MGK001 Megakaryocytic Leukemia 53 0.084
40
SFT003 Soft Tissue Sarcoma 55 0.084
41
LKM001 Leukemoid Reaction 46 0.084
42
P MYC008 Myocarditis 56 0.084
43
P ESS003 Essential Thrombocythemia 66 0.080
44
P MYL005 Myelofibrosis 67 0.080
45
HYP315 Hyperparathyroidism, Neonatal 28 0.080
46
LVR012 Liver Cirrhosis 71 0.080
47
ACQ007 Acquired Immunodeficiency Syndrome 60 0.080
48
END030 End Stage Renal Failure 53 0.080
49
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.076
50
CRH001 Crohn's Disease 76 0.076
51
P KBK002 Kabuki Syndrome 1 49 0.076
52
CRH005 Crohn's Colitis 50 0.076
53
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 13 0.076
54
HDN004 Head and Neck Carcinoma 54 0.076
55
FXP001 Foxp2-Related Speech and Language Disorders 15 0.076
56
HMT002 Hematologic Cancer 62 0.071
57
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.071
58
THY009 Thyroid Lymphoma 48 0.071
59
IMM127 Immune System Cancer 41 0.071
60
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.065
61
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 0.065
62
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.065
63
PLY125 Polycythemia Vera, Somatic 63 0.065
64
P APL001 Aplastic Anemia 74 0.065
65
c EPS035 Episodic Ataxia, Type 2 54 0.065
66
P LVR013 Liver Disease 76 0.065
67
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 62 0.065
68
P LPR003 Leprosy 70 0.065
69
P EPS003 Episodic Ataxia 58 0.065
70
P DYS007 Dyskeratosis Congenita 64 0.065
71
SHW002 Shwachman-Diamond Syndrome 59 0.065
72
EPS004 Episodic Ataxia/myokymia Syndrome 47 0.065
73
GST050 Gastrointestinal System Disease 58 0.065
74
c SRC025 Sarcoidosis 1 58 0.065
75
DFC004 Deficiency Anemia 64 0.065
76
RSP006 Respiratory System Disease 61 0.065
77
P NRV007 Nervous System Disease 71 0.065
78
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.065
79
MYL009 Myelodysplastic Syndrome 73 0.065
80
P DMN001 Diamond-Blackfan Anemia 69 0.065
81
LNG024 Langerhans-Cell Histiocytosis 64 0.065
82
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.065
83
THR042 Thrombocytopenia, X-Linked 46 0.065
84
NTR040 Neutropenia, Cyclic 51 0.065
85
HYP099 Hyperferritinemia-Cataract Syndrome 43 0.065
86
HYP542 Hypersensitivity Syndrome, Carbamazepine-Induced 51 0.065
87
c SPN309 Spinocerebellar Ataxia 6 48 0.065
88
CRT002 Cartilage-Hair Hypoplasia 57 0.065
89
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.065
90
c SPN100 Spinocerebellar Ataxia 27 41 0.065
91
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 42 0.065
92
c JVN010 Juvenile Rheumatoid Arthritis 65 0.065
93
P CNJ013 Conjunctivitis 65 0.065
94
BHC003 Behcet Syndrome 60 0.065
95
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 40 0.065
96
CHR063 Chronic Mucocutaneous Candidiasis 61 0.065
97
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.065
98
LSH001 Leishmaniasis 63 0.065
99
P ALP009 Alopecia Areata 62 0.065
100
TTN003 Tetanus 62 0.065
101
BRC012 Brucellosis 66 0.065
102
c SBR001 Seborrheic Infantile Dermatitis 36 0.065
103
P MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 35 0.065
104
HSH003 Hashimoto Thyroiditis 55 0.065
105
APH001 Aphthous Stomatitis 62 0.065
106
ALP001 Alopecia Universalis 57 0.065
107
TKY002 Takayasu Arteritis 60 0.065
108
BNM001 Bone Marrow Cancer 56 0.065
109
CNT047 Contact Dermatitis 62 0.065
110
KRT001 Keratoconjunctivitis Sicca 58 0.065
111
IDP024 Idiopathic Inflammatory Myopathy 50 0.065
112
P RBL001 Rubella 54 0.065
113
ALL010 Allergic Contact Dermatitis 58 0.065
114
ERY003 Erythema Multiforme 57 0.065
115
c ATM003 Autoimmune Thyroiditis 59 0.065
116
LST001 Listeriosis 53 0.065
117
SCH014 Schistosomiasis 59 0.065
118
TYP007 Typhoid Fever 61 0.065
119
SPL012 Splenic Disease 48 0.065
120
CMP010 Complex Regional Pain Syndrome 59 0.065
121
c DYS174 Dyskeratosis Congenita, Autosomal Dominant 6 32 0.065
122
P MST009 Mastocytosis 54 0.065
123
PLS007 Plasmodium Falciparum Malaria 56 0.065
124
RCT015 Reactive Arthritis 65 0.065
125
RHM027 Rheumatic Disease 55 0.065
126
CHG001 Chagas Disease 62 0.065
127
PRP030 Purpura 60 0.065
128
FLT011 Felty Syndrome 48 0.065
129
c HPT003 Hepatitis a 55 0.065
130
P NTR004 Neutropenia 59 0.065
131
P MNN013 Meningitis 66 0.065
132
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 34 0.065
133
GGR001 Geographic Tongue 45 0.065
134
IRN001 Iron Deficiency Anemia 51 0.065
135
VSC011 Vasculitis 62 0.065
136
MCN007 Meconium Aspiration Syndrome 52 0.065
137
EXT034 Extrinsic Allergic Alveolitis 58 0.065
138
P TXP001 Toxoplasmosis 61 0.065
139
VGT001 Vogt-Koyanagi-Harada Disease 54 0.065
140
HMR001 Hemorrhagic Thrombocythemia 47 0.065
141
TRN030 Transient Erythroblastopenia of Childhood 35 0.065
142
TXC005 Toxic Shock Syndrome 61 0.065
143
P PRT013 Portal Hypertension 61 0.065
144
c ATM011 Autoimmune Hepatitis 62 0.065
145
ECH003 Echinococcosis 53 0.065
146
CHL123 Chlamydia 60 0.065
147
HMR004 Hemorrhagic Fever with Renal Syndrome 52 0.065
148
c MLT127 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 33 0.065
149
VSC003 Visceral Leishmaniasis 56 0.065
150
P PLM036 Pulmonary Fibrosis 69 0.065
151
P INT068 Intestinal Disease 60 0.065
152
SLC006 Silicosis 53 0.065
153
c VRL010 Viral Hepatitis 60 0.065
154
P LCH002 Lichen Planus 61 0.065
155
GST045 Gastroenteritis 59 0.065
156
MYC002 Mycobacterium Avium Complex Disease 52 0.065
157
TNS005 Tonsillitis 58 0.065
158
DPH001 Diphtheria 55 0.065
159
OCL020 Ocular Cicatricial Pemphigoid 51 0.065
160
HMG002 Hemoglobinuria 49 0.065
161
c CHR092 Chronic Myeloproliferative Disease 50 0.065
162
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.065
163
PRR002 Pure Red-Cell Aplasia 47 0.065
164
VRC001 Varicocele 50 0.065
165
PRS012 Pars Planitis 43 0.065
166
c DYS039 Dyskeratosis Congenita Autosomal Dominant 28 0.065
167
MXD005 Mixed Connective Tissue Disease 63 0.065
168
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.065
169
CNN005 Connective Tissue Disease 60 0.065
170
P HMR012 Hemorrhagic Fever 55 0.065
171
P THR014 Thrombocytopenia 63 0.065
172
TNP002 Tinea Profunda 27 0.065
173
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 37 0.065
174
P SPN052 Spondyloarthropathy 58 0.065
175
FLR002 Filariasis 55 0.065
176
ALV002 Alveolar Echinococcosis 50 0.065
177
PLR001 Pleural Tuberculosis 47 0.065
178
ALL006 Allergic Asthma 59 0.065
179
EXN001 Exanthema Subitum 41 0.065
180
BRN012 Bronchiolitis Obliterans 58 0.065
181
MNG003 Mungan Syndrome 21 0.065
182
CTN007 Cutaneous Leishmaniasis 62 0.065
183
DNG002 Dengue Hemorrhagic Fever 60 0.065
184
c HPT007 Hepatitis E 51 0.065
185
P UVT001 Uveitis 60 0.065
186
ACT200 Acute Monoblastic Leukemia 44 0.065
187
ELS001 Eales Disease 47 0.065
188
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 0.065
189
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.065
190
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 50 0.065
191
P PNC001 Pancytopenia 53 0.065
192
ASB001 Asbestosis 42 0.065
193
FDL002 Food Allergy 56 0.065
194
CLN003 Clonorchiasis 46 0.065
195
c CNG418 Congenital Intrauterine Infection-Like Syndrome 17 0.065
196
IRT001 Iritis 36 0.065
197
CYT005 Cytomegalovirus Retinitis 48 0.065
198
P PNV001 Panuveitis 50 0.065
199
GNT006 Giant Papillary Conjunctivitis 38 0.065
200
P LRY019 Laryngitis 55 0.065
201
VRN004 Vernal Keratoconjunctivitis 48 0.065
202
MCC002 Mucocutaneous Leishmaniasis 45 0.065
203
HYR002 Hoyeraal Hreidarsson Syndrome 37 0.065
204
BRN002 Bronchiolitis 56 0.065
205
NRW001 Norwegian Scabies 31 0.065
206
NPH004 Nephropathia Epidemica 39 0.065
207
P SCL015 Scleritis 49 0.065
208
P BRY005 Beryllium Disease 39 0.065
209
ALC009 Alcoholic Liver Cirrhosis 53 0.065
210
PTY001 Pityriasis Rosea 42 0.065
211
HYP063 Hypersplenism 49 0.065
212
OLG001 Oligospermia 39 0.065
213
c EPS015 Episodic Ataxia, Type 7 22 0.065
214
FLC001 Folic Acid Deficiency Anemia 34 0.065
215
ORL012 Oral Leukoplakia 41 0.065
216
ORL013 Oral Lichen Planus 53 0.065
217
TRY001 Trypanosomiasis 51 0.065
218
JNT002 Joint Disorders 55 0.065
219
CYT008 Cytomegalovirus Infection 51 0.065
220
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.065
221
ALC006 Alcoholic Hepatitis 60 0.065
222
BLD053 Blood Platelet Disease 44 0.065
223
LKP003 Leukoplakia 44 0.065
224
c ANT034 Anterior Uveitis 49 0.065
225
KRT006 Keratoconjunctivitis 51 0.065
226
RFR010 Refractory Anemia 43 0.065
227
OPP002 Opportunistic Mycosis 42 0.065
228
LKC003 Leukocyte Disease 45 0.065
229
P ACT135 Acute Graft Versus Host Disease 52 0.065
230
ORL011 Oral Cancer 53 0.065
231
NNT049 Nontuberculous Mycobacterial Lung Disease 41 0.065
232
P RSM001 Rasmussen Encephalitis 42 0.065
233
c ACT219 Acute Myeloid Leukemia, Flt3-Related 32 0.065
234
c CHR576 Chronic Beryllium Disease 39 0.065
235
LWN001 Lown-Ganong-Levine Syndrome 28 0.065
236
EGG001 Egg Allergy 44 0.065
237
EWN002 Ewing's Family of Tumors 45 0.065
238
BNN003 Bone Inflammation Disease 46 0.065
239
PRS036 Parasitic Protozoa Infectious Disease 45 0.065
240
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 26 0.065
241
CCC002 Coccidiosis 49 0.065
242
HMN032 Human Herpesvirus 8 42 0.065
243
c INT064 Intermediate Uveitis 47 0.065
244
PST053 Postherpetic Neuralgia 41 0.065
245
PRN021 Paranasal Sinus Disease 50 0.065
246
NRT004 Neuritis 52 0.065
247
P CHL066 Cholangitis 48 0.065
248
KLD001 Keloids 50 0.065
249
ANC002 Anca-Associated Vasculitis 43 0.065
250
CPL004 Caplan's Syndrome 32 0.065
251
END018 Endometrium Carcinoma in Situ 25 0.065
252
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 41 0.065
253
FSR001 Fusariosis 31 0.065
254
MCR191 Microscopic Colitis 46 0.065
255
P SCL009 Sclerosing Cholangitis 47 0.065
256
DRG002 Drug-Induced Hepatitis 39 0.065
257
ECT004 Ecthyma 37 0.065
258
ANM001 Anemia of Prematurity 44 0.065
259
LCH004 Lichen Disease 37 0.065
260
P PNM006 Pneumoconiosis 51 0.065
261
ESN004 Eosinophilic Gastritis 41 0.065
262
c DYS040 Dyskeratosis Congenita Autosomal Recessive 22 0.065
263
P PMP005 Pemphigus Vulgaris 47 0.065
264
SNL007 Senile Cataract 37 0.065
265
CRD137 Cardiogenic Shock 44 0.065
266
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 22 0.065
267
NNL002 Nonalcoholic Steatohepatitis 49 0.065
268
CYC007 Cyclic Thrombocytopenia 37 0.065
269
ACT064 Acute Necrotizing Encephalitis 27 0.065
270
OTP003 Oto-Palatal-Digital Syndrome 14 0.065
271
P RFR008 Refractory Anemia with Excess Blasts 30 0.065
272
HYP457 Hypertrophic Scars 45 0.065
273
MYC022 Mycoplasmal Pneumonia 32 0.065
274
STC004 Stachybotrys Chartarum 38 0.065
275
EXT035 Extrinsic Cardiomyopathy 38 0.065
276
PLY020 Polyradiculoneuropathy 42 0.065
277
IDP064 Idiopathic Neutropenia 43 0.065
278
c PRM225 Primary Thrombocytopenia 42 0.065
279
CRV045 Cervical Intraepithelial Neoplasia 41 0.065
280
OLG015 Oligoarticular Juvenile Arthritis 39 0.065
281
ORF044 Orofacial Granulomatosis 35 0.065
282
TRC006 Trichosporonosis 29 0.065
283
c TYP024 Type Ii Mixed Cryoglobulinemia 35 0.065
284
ATP013 Atopic Keratoconjunctivitis 34 0.065
285
c ACT036 Acute Cholangitis 31 0.065
286
IDP074 Idiopathic Bronchiectasis 34 0.065
287
STR072 Stromal Keratitis 41 0.065
288
ATM012 Autoimmune Disease of Blood 36 0.065
289
DSS024 Disease of Anatomical Entity 40 0.065
290
PRM025 Primary Bacterial Infectious Disease 42 0.065
291
INH011 Inherited Bone Marrow Failure Syndromes 24 0.065
292
TRC034 Torch Syndrome 12 0.065
293
VBR003 Vibrio Vulnificus Infection 23 0.065
294
CHR415 Chronic Venous Leg Ulcers 31 0.065
295
BCH003 Boucher-Neuhauser Syndrome 27 0.060