Search results for hyperparathyroidism, neonatal severe primary

238 hits were found for hyperparathyroidism, neonatal severe primary

# Family MCID Name MIFTS Score
1
HYP315 Hyperparathyroidism, Neonatal 37 6.634
2
P HYP069 Hyperparathyroidism 56 0.917
3
P KDN018 Kidney Disease 65 0.272
4
ADN018 Adenoma 58 0.270
5
P HPT021 Hepatitis 68 0.269
6
P THY032 Thyroiditis 53 0.265
7
P PNC044 Pancreatitis 60 0.241
8
BNS002 Bone Structure Disease 36 0.217
9
PRT029 Parathyroid Adenoma 49 0.216
10
P HYP086 Hypothyroidism 60 0.213
11
P ART022 Arthritis 72 0.196
12
END072 Endotheliitis 41 0.188
13
URN009 Urinary System Disease 49 0.186
14
P BRS047 Breast Cancer 100 0.183
15
NRN002 Neuronitis 39 0.180
16
P THR014 Thrombocytopenia 63 0.178
17
P OBS005 Obesity 91 0.176
18
P LKM002 Leukemia 72 0.174
19
PRT036 Peritonitis 60 0.174
20
MTH009 Mouth Disease 62 0.173
21
PHY002 Physical Disorder 43 0.159
22
BRT030 Birth Defects 44 0.159
23
P FML068 Familial Hypocalciuric Hypercalcemia 47 0.156
24
P ADN016 Adenocarcinoma 69 0.155
25
IMP003 Impaired Renal Function Disease 36 0.154
26
P LPS004 Lupus Erythematosus 63 0.151
27
P CRV039 Cervicitis 45 0.151
28
MLN008 Melanoma 70 0.146
29
MDS022 Mediastinitis 40 0.145
30
NLL002 Null Syndrome 26 0.143
31
P OST002 Osteoporosis 63 0.141
32
c HYP615 Hyperparathyroidism, Familial Primary 53 0.140
33
c ACT027 Acute Pancreatitis 56 0.139
34
P HYP729 Hypersensitivity Reaction Disease 43 0.137
35
c CHR089 Chronic Kidney Failure 65 0.131
36
P RHM011 Rheumatoid Arthritis 87 0.130
37
P MYC007 Myocardial Infarction 77 0.130
38
P HYP065 Hyperaldosteronism 50 0.130
39
P HYP076 Hyperthyroidism 53 0.127
40
CLT003 Colitis 58 0.127
41
P AMY004 Amyloidosis 64 0.126
42
c PND001 Pain Disorder 55 0.126
43
MNT002 Mental Depression 52 0.123
44
NPH003 Nephrocalcinosis 47 0.123
45
ADJ001 Adjustment Disorder 38 0.123
46
PRS047 Prostatitis 55 0.123
47
P HYP024 Hypoparathyroidism 52 0.121
48
ART111 Artery Disease 55 0.121
49
ANX002 Anxiety Disorder 66 0.121
50
P MYP004 Myopathy 68 0.119
51
END030 End Stage Renal Failure 51 0.117
52
c SYS001 Systemic Lupus Erythematosus 86 0.116
53
DDN006 Duodenitis 40 0.115
54
P RCK004 Rickets 57 0.114
55
CYS001 Cystic Fibrosis 86 0.114
56
ULC004 Ulcerative Colitis 72 0.113
57
c HPT016 Hepatitis B 62 0.113
58
GTR002 Goiter 52 0.112
59
P SPS003 Spastic Diplegia 52 0.111
60
TBR010 Tuberculosis 69 0.111
61
HYP025 Hyperphosphatemia 46 0.110
62
P ORL007 Oral Cavity Cancer 57 0.110
63
PCK002 Pick Disease 68 0.110
64
ALR002 Al-Raqad Syndrome 29 0.109
65
PNC001 Pancytopenia 49 0.108
66
P DRR001 Diarrhea 59 0.107
67
ORL011 Oral Cancer 56 0.106
68
CNG034 Congestive Heart Failure 70 0.104
69
P INF032 Infertility 57 0.104
70
RNL007 Renal Tubular Acidosis 48 0.104
71
END035 Endocrine Gland Cancer 50 0.103
72
VND001 Vein Disease 49 0.102
73
ATH003 Atherosclerosis 65 0.101
74
P DBT005 Diabetes Insipidus 52 0.100
75
URM002 Uremia 48 0.100
76
LVR012 Liver Cirrhosis 66 0.099
77
BNF002 Bone Fracture 51 0.098
78
P CNJ013 Conjunctivitis 63 0.097
79
PRM097 Primary Immunodeficiency Disease 64 0.096
80
P MLT019 Multiple Myeloma 82 0.096
81
CLC006 Calcinosis 49 0.095
82
P PHC003 Pheochromocytoma 72 0.094
83
P GLM007 Glomerulonephritis 55 0.093
84
c HPT001 Hepatitis C 62 0.093
85
BLD054 Blood Protein Disease 39 0.092
86
VGN023 Vaginitis 41 0.092
87
P LRY019 Laryngitis 53 0.092
88
P PSD015 Pseudohypoparathyroidism 46 0.092
89
MTB004 Metabolic Acidosis 47 0.091
90
MSC004 Muscle Tissue Disease 37 0.090
91
P PLY018 Polycythemia 56 0.090
92
P HYP060 Hyperinsulinism 57 0.089
93
P GRV001 Graves' Disease 57 0.089
94
P NPH009 Nephrolithiasis 55 0.086
95
AND005 Androgen Insensitivity Syndrome, Mild 16 0.086
96
P HYP265 Hypotonia 39 0.085
97
P MSC033 Muscle Disorders 52 0.084
98
P AST007 Astrocytoma 63 0.083
99
ALP008 Alopecia 54 0.082
100
P HMN010 Hemangioma 59 0.081
101
SCK005 Sickle Cell Disease 51 0.079
102
VTM003 Vitamin Metabolic Disorder 31 0.079
103
P CLC005 Celiac Disease 69 0.078
104
NTR005 Nutritional Deficiency Disease 47 0.078
105
OVR063 Overnutrition 48 0.077
106
HPT074 Hepatic Adenoma, Somatic 44 0.077
107
P GNT008 Giant Cell Tumor 48 0.076
108
SPS057 Spasticity 42 0.076
109
P HYP035 Hypophosphatasia 57 0.075
110
NSD001 Nose Disease 49 0.074
111
DWR001 Dwarfism 45 0.073
112
c CLL013 Cell Type Cancer 48 0.073
113
INS001 Insulinoma 60 0.073
114
P GST044 Gastritis 55 0.073
115
c TRC078 Trichohepatoenteric Syndrome 2 34 0.072
116
HYP005 Hypokalemia 50 0.072
117
P FNC004 Fanconi Syndrome 48 0.071
118
BND014 Bone Development Disease 39 0.070
119
FBR054 Fibroma 41 0.070
120
P LNG028 Long Qt Syndrome 64 0.069
121
GRW007 Growth Hormone Deficiency 48 0.069
122
PLM010 Pulmonary Edema 52 0.068
123
P PLY019 Polyneuropathy 54 0.068
124
GST019 Gastrointestinal Stromal Tumor 74 0.068
125
MNR003 Mineral Metabolism Disease 40 0.068
126
P OST005 Osteogenesis Imperfecta 68 0.067
127
P TRC086 Trichohepatoenteric Syndrome 1 51 0.067
128
PLM033 Pulmonary Embolism 59 0.066
129
STM006 Stomach Disease 47 0.066
130
HNM002 Hinman Syndrome 27 0.066
131
P THY023 Thymoma 59 0.066
132
P TBR001 Tuberous Sclerosis 67 0.066
133
MRB003 Morbid Obesity 58 0.066
134
SKL017 Skeletal Dysplasias 44 0.065
135
GLC003 Glucose Intolerance 54 0.065
136
P PYL005 Pyelonephritis 52 0.064
137
FBR009 Fibrous Dysplasia 44 0.064
138
SKL014 Skeletal Dysplasia 46 0.064
139
CHL004 Cholelithiasis 47 0.063
140
PPL022 Papilloma 54 0.063
141
PSR001 Psoriatic Arthritis 63 0.063
142
P MYT002 Myotonic Dystrophy 48 0.063
143
MYX004 Myxedema 34 0.062
144
PRT014 Protein S Deficiency 51 0.062
145
URT039 Urticaria 56 0.061
146
VSC006 Vascular Cancer 52 0.061
147
P ICH004 Ichthyosis 53 0.061
148
PHR003 Pharyngitis 53 0.061
149
BNM008 Bone Mineral Density, Low 17 0.061
150
MTR014 Motor Neuron Disease 56 0.061
151
P SPN052 Spondyloarthropathy 59 0.060
152
P TRN020 Turner Syndrome 65 0.060
153
THY030 Thyroid Gland Disease 49 0.060
154
PRP016 Paraplegia 48 0.060
155
P PRC031 Preeclampsia/eclampsia 1 55 0.059
156
SPC003 Specific Developmental Disorder 38 0.058
157
HMN009 Hemangioblastoma 45 0.058
158
ARC002 Arachnoiditis 41 0.057
159
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.057
160
ADR009 Adrenal Cortex Disease 39 0.057
161
APR001 Apraxia 49 0.057
162
P CSH001 Cushing's Syndrome 65 0.056
163
P DDN001 Duodenal Ulcer 48 0.056
164
BNN003 Bone Inflammation Disease 45 0.056
165
CRB025 Carbohydrate Metabolic Disorder 47 0.055
166
ART017 Aortic Disease 57 0.055
167
ISL001 Islet Cell Tumor 48 0.055
168
LPD007 Lipoadenoma 29 0.055
169
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.054
170
P ATR005 Atrophic Gastritis 47 0.054
171
P PRC019 Precocious Puberty 50 0.054
172
IMP004 Impetigo 42 0.053
173
LCT002 Lactose Intolerance 43 0.053
174
P ART034 Aortopulmonary Window 22 0.052
175
ORL015 Oral Squamous Cell Carcinoma 55 0.052
176
CTS003 Coats Disease 58 0.052
177
SRT004 Serotonin Syndrome 47 0.051
178
PRN011 Pernicious Anemia 43 0.051
179
ALX003 Alexander Disease 65 0.050
180
c HMG001 Hemoglobin C Disease 44 0.050
181
P NRF018 Neurofibromatosis, Type 1 78 0.050
182
RNL078 Renal Dysplasia 50 0.050
183
c HYP317 Hypocalciuric Hypercalcemia, Type Ii 39 0.049
184
P PRG013 Paraganglioma 54 0.049
185
ARC007 Arachnoid Cysts 38 0.049
186
GST023 Gastric Ulcer 54 0.049
187
PMS001 Poems Syndrome 51 0.049
188
GST078 Gastrointestinal Allergy 39 0.048
189
VSC044 Visceral Myopathy 48 0.048
190
HYP068 Hyperostosis 38 0.048
191
PPT005 Peptic Ulcer Disease 57 0.047
192
P PTT014 Pitt-Hopkins Syndrome 51 0.047
193
c HYP314 Hypocalciuric Hypercalcemia, Type I 39 0.046
194
CYS039 Cystic Kidney Disease 50 0.046
195
c BLD124 Bleeding Disorder, Platelet-Type, 11 36 0.046
196
ADR005 Adrenal Carcinoma 54 0.046
197
ESN011 Eisenmenger Syndrome 46 0.046
198
SPS019 Spastic Paraparesis 34 0.045
199
CYS013 Cystinuria 63 0.045
200
P ART084 Arteriovenous Fistula 43 0.045
201
OST015 Osteochondrodysplasia 52 0.045
202
LWS003 Lowe Syndrome 59 0.044
203
P MYM002 Moyamoya Disease 60 0.044
204
CRR007 Cirrhosis, Cryptogenic 43 0.044
205
VSC047 Vascular Malformation 43 0.043
206
P PNL012 Penile Cancer 54 0.042
207
P BRC006 Brachydactyly 55 0.041
208
P ATX010 Ataxia Neuropathy Spectrum 27 0.041
209
P HYP192 Hypocalcemia, Autosomal Dominant 58 0.041
210
P HYP057 Hypervitaminosis D 38 0.041
211
c HMG004 Hemoglobin D Disease 33 0.041
212
ALK013 Alkaptonuria 54 0.040
213
CHN054 Chondrodysplasia, Blomstrand Type 42 0.040
214
P GCH001 Gaucher's Disease 63 0.040
215
ORP003 Oropharynx Cancer 46 0.040
216
P CHN059 Chondrocalcinosis 44 0.040
217
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.039
218
CRV030 Cervical Adenitis 30 0.039
219
c SPN225 Spondyloarthropathy 1 61 0.039
220
SCL022 Scleredema 24 0.038
221
CYS010 Cystinosis 53 0.038
222
RGH009 Right Atrial Isomerism 48 0.038
223
P FNC043 Fanconi Anemia, Complementation Group E 51 0.038
224
PLM017 Pulmonary Alveolar Microlithiasis 46 0.038
225
P PND002 Pendred Syndrome 56 0.037
226
c PRM023 Pre-Malignant Neoplasm 43 0.037
227
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 35 0.037
228
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 30 0.036
229
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 43 0.036
230
c MCL062 Mucolipidosis Ii Alpha/beta 50 0.036
231
GLL008 Gilles De La Tourette Syndrome 63 0.036
232
c FML303 Familial/multiple Cancer 16 0.035
233
PLM032 Pulmonary Blastoma 49 0.035
234
c OST126 Osteopetrosis, Autosomal Recessive 1 36 0.034
235
c GRV008 Graves Disease 1 44 0.034
236
RNL077 Renal Fibrosis 46 0.033
237
HRL006 Harel-Yoon Syndrome 25 0.032
238
P TRC072 Treacher Collins Syndrome 1 54 0.030
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