Search results for hyperparathyroidism, neonatal severe primary

246 hits were found for hyperparathyroidism, neonatal severe primary

# Family MCID Name MIFTS Score
1
HYP776 Hyperparathyroidism, Neonatal Severe 39 7.455
2
P HYP069 Hyperparathyroidism 58 1.003
3
c PRM005 Primary Hyperparathyroidism 59 0.748
4
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.418
5
ADN018 Adenoma 63 0.297
6
P KDN018 Kidney Disease 69 0.295
7
P THY032 Thyroiditis 56 0.288
8
P HPT021 Hepatitis 75 0.287
9
P HYP726 Hypercalcemia, Infantile, 1 57 0.276
10
P PNC044 Pancreatitis 64 0.260
11
AGN016 Aging 65 0.254
12
P HYP086 Hypothyroidism 62 0.250
13
c BLD140 Blood Group, I System 37 0.240
14
PRT029 Parathyroid Adenoma 50 0.235
15
c CHR089 Chronic Kidney Failure 72 0.229
16
P DBT009 Diabetes Mellitus 72 0.214
17
END072 Endotheliitis 46 0.205
18
P ART022 Arthritis 77 0.205
19
URN009 Urinary System Disease 58 0.204
20
P BRS047 Breast Cancer 100 0.203
21
NRN002 Neuronitis 43 0.201
22
P THR014 Thrombocytopenia 65 0.196
23
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.196
24
P LKM002 Leukemia 75 0.191
25
PRT036 Peritonitis 67 0.190
26
P FML068 Familial Hypocalciuric Hypercalcemia 49 0.172
27
P ADN016 Adenocarcinoma 71 0.171
28
P LPS004 Lupus Erythematosus 69 0.167
29
P CRV039 Cervicitis 49 0.164
30
MDS022 Mediastinitis 44 0.163
31
MLN008 Melanoma 72 0.163
32
c MLT156 Multiple Endocrine Neoplasia, Type I 70 0.156
33
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.156
34
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.156
35
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.155
36
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.155
37
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.155
38
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.155
39
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.155
40
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.155
41
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.155
42
P OST002 Osteoporosis 75 0.155
43
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.151
44
P AMY004 Amyloidosis 69 0.148
45
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.147
46
P ANR048 Aniridia 1 68 0.143
47
P HYP076 Hyperthyroidism 56 0.142
48
ANR038 Anorexia Nervosa 1 21 0.141
49
BLD137 Blood Group--Ahonen 17 0.141
50
P MYC007 Myocardial Infarction 81 0.140
51
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.140
52
P LNG032 Lung Cancer 99 0.140
53
P MYL005 Myelofibrosis 75 0.140
54
ANX010 Anxiety 72 0.138
55
CLT003 Colitis 63 0.134
56
NPH003 Nephrocalcinosis 49 0.133
57
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.133
58
P RHM011 Rheumatoid Arthritis 91 0.132
59
DDN006 Duodenitis 46 0.132
60
P MYP004 Myopathy 69 0.131
61
MNT002 Mental Depression 60 0.131
62
c SYS001 Systemic Lupus Erythematosus 86 0.131
63
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.130
64
P HYP024 Hypoparathyroidism 55 0.130
65
RCK004 Rickets 63 0.127
66
PRS047 Prostatitis 59 0.127
67
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.126
68
CYS001 Cystic Fibrosis 85 0.126
69
ANR040 Aneurysm 61 0.126
70
GTR002 Goiter 53 0.125
71
END030 End Stage Renal Failure 59 0.125
72
ALR002 Al-Raqad Syndrome 30 0.123
73
PNC001 Pancytopenia 50 0.122
74
P INF032 Infertility 59 0.118
75
P RNL007 Renal Tubular Acidosis 51 0.118
76
SPS003 Spastic Diplegia 55 0.118
77
HYP025 Hyperphosphatemia 48 0.118
78
c HPT016 Hepatitis B 68 0.117
79
ENT004 Enthesopathy 38 0.113
80
P DRR001 Diarrhea 60 0.113
81
P CNJ013 Conjunctivitis 67 0.111
82
LVR012 Liver Cirrhosis 73 0.110
83
CNG034 Congestive Heart Failure 74 0.110
84
P DBT005 Diabetes Insipidus 54 0.110
85
BNF002 Bone Fracture 56 0.108
86
URM002 Uremia 52 0.108
87
CLC006 Calcinosis 51 0.107
88
MYL069 Myeloma, Multiple 86 0.105
89
THY028 Thyroid Cancer 72 0.105
90
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.105
91
VGN023 Vaginitis 59 0.105
92
MTB004 Metabolic Acidosis 49 0.103
93
P LRY019 Laryngitis 57 0.103
94
P PLY018 Polycythemia 60 0.102
95
P GLM007 Glomerulonephritis 61 0.102
96
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.101
97
P PHC003 Pheochromocytoma 72 0.101
98
P PSD015 Pseudohypoparathyroidism 50 0.100
99
P MYC084 Mycobacterium Tuberculosis 1 69 0.100
100
NPH009 Nephrolithiasis 57 0.100
101
P GRV001 Graves' Disease 62 0.097
102
c HPT001 Hepatitis C 73 0.096
103
HYP060 Hyperinsulinism 56 0.095
104
HPT082 Hepatic Adenomas, Familial 52 0.093
105
P HMN010 Hemangioma 61 0.093
106
P HYP265 Hypotonia 40 0.092
107
P AST007 Astrocytoma 66 0.091
108
ALP046 Alport Syndrome, X-Linked 74 0.091
109
SCK005 Sickle Cell Disease 54 0.091
110
SPS057 Spasticity 41 0.088
111
c GRV008 Graves Disease 1 52 0.087
112
P FNC004 Fanconi Syndrome 54 0.086
113
P CLC063 Celiac Disease 1 65 0.085
114
MCC012 Mccune-Albright Syndrome 65 0.084
115
P ALP008 Alopecia 56 0.084
116
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.084
117
BLD163 Blood Group, Dombrock System 23 0.084
118
PPL002 Papillary Carcinoma 51 0.083
119
P THY109 Thyroid Cancer, Nonmedullary, 1 64 0.083
120
c ART101 Aortic Valve Disease 2 65 0.083
121
OVR063 Overnutrition 53 0.082
122
INS001 Insulinoma 66 0.082
123
P GNT008 Giant Cell Tumor 49 0.082
124
CNN003 Conn's Syndrome 70 0.082
125
CNS004 Constipation 57 0.081
126
c SML038 Small Cell Cancer of the Lung 67 0.080
127
P GST044 Gastritis 61 0.080
128
PLM033 Pulmonary Embolism 62 0.079
129
P LNG028 Long Qt Syndrome 63 0.079
130
P HYP035 Hypophosphatasia 58 0.079
131
PHR003 Pharyngitis 59 0.077
132
BRT054 Brittle Bone Disorder 67 0.077
133
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.077
134
c TRC078 Trichohepatoenteric Syndrome 2 34 0.077
135
P TBR001 Tuberous Sclerosis 69 0.077
136
P PLY019 Polyneuropathy 58 0.076
137
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.076
138
DWR001 Dwarfism 48 0.076
139
MTR014 Motor Neuron Disease 62 0.076
140
GST019 Gastrointestinal Stromal Tumor 74 0.075
141
P THY023 Thymoma 65 0.075
142
HYP005 Hypokalemia 53 0.075
143
P MLT008 Multinodular Goiter 44 0.075
144
MRB003 Morbid Obesity 61 0.075
145
CHL004 Cholelithiasis 51 0.074
146
GLC003 Glucose Intolerance 58 0.074
147
P RNL045 Renal Tubular Acidosis, Distal 42 0.073
148
SKL017 Skeletal Dysplasias 48 0.073
149
MYX004 Myxedema 44 0.072
150
P TRC086 Trichohepatoenteric Syndrome 1 54 0.072
151
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.072
152
THY030 Thyroid Gland Disease 51 0.072
153
URT039 Urticaria 59 0.071
154
PRP016 Paraplegia 53 0.071
155
P LTR001 Lateral Sclerosis 58 0.071
156
PLM010 Pulmonary Edema 57 0.071
157
FBR009 Fibrous Dysplasia 49 0.071
158
P HMN036 Hemangiopericytoma, Malignant 52 0.070
159
GRW007 Growth Hormone Deficiency 52 0.069
160
HMN009 Hemangioblastoma 56 0.069
161
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.069
162
PPL022 Papilloma 58 0.069
163
P ICH004 Ichthyosis 54 0.069
164
c BRN108 Branchiootic Syndrome 1 47 0.068
165
P MYT002 Myotonic Dystrophy 50 0.068
166
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 0.067
167
P TRN020 Turner Syndrome 69 0.066
168
HLC007 Helicobacter Pylori Infection 64 0.065
169
P PYL005 Pyelonephritis 56 0.064
170
NDL007 Nodular Goiter 50 0.064
171
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 35 0.064
172
P ART034 Aortopulmonary Window 25 0.063
173
PRT014 Protein S Deficiency 47 0.062
174
ARC002 Arachnoiditis 45 0.062
175
PRN011 Pernicious Anemia 50 0.062
176
P DDN001 Duodenal Ulcer 53 0.061
177
APR001 Apraxia 52 0.060
178
EXP004 Exophthalmos 50 0.060
179
P PTT014 Pitt-Hopkins Syndrome 52 0.059
180
OST003 Osteonecrosis 63 0.059
181
P BRT004 Bartter Disease 52 0.058
182
P PRG013 Paraganglioma 57 0.058
183
c INT072 Intestinal Pseudo-Obstruction 57 0.058
184
IMP004 Impetigo 45 0.058
185
ALK013 Alkaptonuria 56 0.058
186
FLL031 Follicular Adenoma 41 0.057
187
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.057
188
P PRC019 Precocious Puberty 52 0.057
189
SPS019 Spastic Paraparesis 33 0.057
190
RNL078 Renal Dysplasia 49 0.057
191
CRP001 Carpal Tunnel Syndrome 64 0.057
192
HYP730 Hypogonadotropic Hypogonadism 56 0.056
193
ISL001 Islet Cell Tumor 54 0.056
194
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.056
195
P LCT002 Lactose Intolerance 48 0.056
196
ADR005 Adrenal Carcinoma 59 0.056
197
CRC006 Carcinoid Syndrome 59 0.055
198
P ART084 Arteriovenous Fistula 46 0.055
199
P TRC072 Treacher Collins Syndrome 1 61 0.055
200
CYS013 Cystinuria 64 0.055
201
ARC007 Arachnoid Cysts 39 0.054
202
PLM017 Pulmonary Alveolar Microlithiasis 48 0.054
203
SRT004 Serotonin Syndrome 51 0.053
204
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 38 0.052
205
P FNC043 Fanconi Anemia, Complementation Group E 52 0.052
206
IDP073 Idiopathic Hypercalciuria 46 0.052
207
P ACT150 Acute Adrenal Insufficiency 51 0.052
208
PRR002 Pure Red-Cell Aplasia 52 0.052
209
PRS037 Periostitis 33 0.051
210
HYP068 Hyperostosis 52 0.051
211
CYS039 Cystic Kidney Disease 49 0.050
212
LWC002 Lowe Oculocerebrorenal Syndrome 62 0.050
213
SPN331 Spondyloocular Syndrome 34 0.049
214
ESN011 Eisenmenger Syndrome 49 0.049
215
P GCH001 Gaucher's Disease 62 0.049
216
c TBR025 Tuberous Sclerosis 1 63 0.049
217
PTT009 Pituitary Gland Disease 56 0.049
218
P BRC006 Brachydactyly 57 0.049
219
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 38 0.049
220
c HYP057 Hypervitaminosis D 40 0.048
221
SCL022 Scleredema 27 0.048
222
HYP029 Hyperthyroxinemia 27 0.047
223
OST015 Osteochondrodysplasia 54 0.047
224
END028 Endemic Goiter 40 0.047
225
HYP780 Hypoadrenocorticism, Familial 59 0.045
226
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.045
227
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.044
228
PLM011 Plummer's Disease 38 0.044
229
PPT002 Peptic Ulcer Perforation 38 0.044
230
EPD070 Epidermoid Cysts 46 0.044
231
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.044
232
c ATM068 Autoimmune Hypoparathyroidism 30 0.044
233
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.043
234
P RNL015 Renal Hypertension 46 0.042
235
c CRN243 Carney Complex, Type 1 35 0.042
236
CHN054 Chondrodysplasia, Blomstrand Type 45 0.042
237
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.042
238
P ANX007 Anauxetic Dysplasia 1 36 0.041
239
CYS010 Cystinosis 55 0.041
240
P TWN003 Townes-Brocks Syndrome 57 0.040
241
c ALZ056 Alzheimer Disease 3 41 0.040
242
P MYM013 Moyamoya Disease 1 50 0.039
243
P THR117 Three M Syndrome 1 52 0.039
244
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 24 0.038
245
P MYS033 Miyoshi Muscular Dystrophy 1 48 0.033
246
CRV030 Cervical Adenitis 33 0.032
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