Search results for "hyperparathyroidism, neonatal severe primary"

The MalaCard for "hyperparathyroidism, neonatal severe primary" has been retired.
Searching MalaCards for entries containing "hyperparathyroidism, neonatal severe primary"

287 hits were found for 'hyperparathyroidism, neonatal severe primary'

# Family MCID Name MIFTS Score
1
HYP315 Hyperparathyroidism, Neonatal 33 7.011
2
P HYP069 Hyperparathyroidism 57 0.954
3
P HPT021 Hepatitis 70 0.277
4
ADN018 Adenoma 59 0.277
5
P THY032 Thyroiditis 54 0.271
6
P PNC044 Pancreatitis 60 0.249
7
P HYP086 Hypothyroidism 65 0.228
8
PRT029 Parathyroid Adenoma 47 0.221
9
PRT030 Parathyroid Gland Disease 49 0.216
10
c HYP615 Hyperparathyroidism, Familial Primary 55 0.212
11
END072 Endotheliitis 42 0.194
12
P ART022 Arthritis 75 0.192
13
NTR005 Nutritional Deficiency Disease 39 0.191
14
NRN002 Neuronitis 42 0.186
15
P BRS047 Breast Cancer 100 0.182
16
BNS002 Bone Structure Disease 36 0.182
17
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.182
18
P THR014 Thrombocytopenia 64 0.180
19
P LKM002 Leukemia 70 0.179
20
PRT036 Peritonitis 62 0.178
21
P HRT032 Heart Disease 76 0.172
22
P OBS005 Obesity 93 0.171
23
IMP003 Impaired Renal Function Disease 37 0.168
24
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.165
25
c CHR089 Chronic Kidney Failure 66 0.161
26
P CRV039 Cervicitis 44 0.156
27
P FML068 Familial Hypocalciuric Hypercalcemia 38 0.156
28
P LPS004 Lupus Erythematosus 63 0.155
29
P LVR013 Liver Disease 72 0.149
30
MDS022 Mediastinitis 41 0.147
31
P ADN016 Adenocarcinoma 69 0.146
32
P RCK004 Rickets 59 0.143
33
P MYP004 Myopathy 67 0.141
34
c ACT027 Acute Pancreatitis 56 0.141
35
P RHM011 Rheumatoid Arthritis 88 0.139
36
ADJ001 Adjustment Disorder 38 0.138
37
P HYP065 Hyperaldosteronism 51 0.135
38
P HYP076 Hyperthyroidism 56 0.133
39
BRT030 Birth Defects 43 0.132
40
MRC001 Marchiafava Bignami Disease 50 0.132
41
MTH009 Mouth Disease 63 0.132
42
P MYC007 Myocardial Infarction 79 0.132
43
ACD009 Acid-Labile Subunit, Deficiency of 48 0.130
44
c PND001 Pain Disorder 55 0.130
45
END035 Endocrine Gland Cancer 52 0.129
46
END030 End Stage Renal Failure 52 0.129
47
CLT003 Colitis 59 0.129
48
P AMY004 Amyloidosis 64 0.128
49
ACR041 Acromelic Frontonasal Dysostosis 46 0.128
50
P MYL005 Myelofibrosis 67 0.126
51
P HYP237 Hypercalcemia, Infantile 51 0.124
52
PRS047 Prostatitis 56 0.124
53
P HYP024 Hypoparathyroidism 52 0.122
54
ALR002 Al-Raqad Syndrome 36 0.122
55
GST050 Gastrointestinal System Disease 54 0.121
56
NPH003 Nephrocalcinosis 46 0.120
57
c SYS001 Systemic Lupus Erythematosus 87 0.120
58
URN009 Urinary System Disease 53 0.119
59
P URF003 Urofacial Syndrome 1 52 0.119
60
PHY002 Physical Disorder 44 0.119
61
DDN006 Duodenitis 44 0.118
62
P PNC001 Pancytopenia 52 0.117
63
c HPT016 Hepatitis B 64 0.116
64
CYS001 Cystic Fibrosis 86 0.116
65
GTR002 Goiter 54 0.115
66
VSC007 Vascular Disease 67 0.114
67
ULC004 Ulcerative Colitis 75 0.113
68
P SPS003 Spastic Diplegia 53 0.112
69
HYP025 Hyperphosphatemia 46 0.112
70
P ENC004 Encephalitis 61 0.112
71
TBR010 Tuberculosis 69 0.111
72
VND001 Vein Disease 52 0.111
73
PCK002 Pick Disease 67 0.110
74
P DRR001 Diarrhea 51 0.110
75
P NRV007 Nervous System Disease 71 0.109
76
RNL007 Renal Tubular Acidosis 50 0.109
77
CNG034 Congestive Heart Failure 71 0.108
78
PRM097 Primary Immunodeficiency Disease 61 0.107
79
HPT023 Hepatocellular Carcinoma 91 0.107
80
GRW007 Growth Hormone Deficiency 48 0.106
81
BLD054 Blood Protein Disease 40 0.106
82
LRN003 Learning Disability 51 0.105
83
BNF002 Bone Fracture 47 0.102
84
URM002 Uremia 50 0.102
85
LVR012 Liver Cirrhosis 67 0.102
86
ATH003 Atherosclerosis 62 0.101
87
ANX002 Anxiety Disorder 69 0.101
88
ALN001 Aland Island Eye Disease 45 0.100
89
P CHR345 Chronic Pain 49 0.100
90
P CNJ013 Conjunctivitis 65 0.100
91
P DBT005 Diabetes Insipidus 53 0.100
92
P APL001 Aplastic Anemia 73 0.099
93
NSD001 Nose Disease 52 0.099
94
c HPT001 Hepatitis C 68 0.099
95
CLC006 Calcinosis 49 0.099
96
VTM003 Vitamin Metabolic Disorder 33 0.098
97
KRT002 Keratomalacia 54 0.097
98
P GLM007 Glomerulonephritis 56 0.096
99
HDN002 Head Injury 45 0.096
100
VGN023 Vaginitis 42 0.096
101
MTB004 Metabolic Acidosis 48 0.095
102
P LRY019 Laryngitis 55 0.094
103
c MLT136 Multiple Endocrine Neoplasia 1 68 0.094
104
P PSD015 Pseudohypoparathyroidism 44 0.093
105
P NPH009 Nephrolithiasis 60 0.093
106
MDD011 Mood Disorder 61 0.092
107
CHR005 Chorioamnionitis 48 0.092
108
P NRV006 Nervous System Cancer 62 0.092
109
P HYP060 Hyperinsulinism 59 0.091
110
P PLY018 Polycythemia 57 0.091
111
P PHC003 Pheochromocytoma 71 0.091
112
P GRV001 Graves' Disease 61 0.091
113
MNR003 Mineral Metabolism Disease 41 0.090
114
SPC003 Specific Developmental Disorder 40 0.089
115
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.088
116
STM006 Stomach Disease 50 0.088
117
ACR002 Acrocapitofemoral Dysplasia 36 0.087
118
BND014 Bone Development Disease 42 0.087
119
LPD004 Lipoid Nephrosis 48 0.087
120
LPD008 Lipid Metabolism Disorder 58 0.086
121
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.084
122
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.084
123
P HMN010 Hemangioma 60 0.083
124
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.083
125
SCK005 Sickle Cell Disease 49 0.083
126
MSC004 Muscle Tissue Disease 36 0.083
127
c INF071 Inflammatory Bowel Disease 1 51 0.082
128
ALP008 Alopecia 55 0.082
129
P TXP001 Toxoplasmosis 60 0.082
130
P CLC005 Celiac Disease 67 0.081
131
ART021 Arteriosclerosis 59 0.080
132
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.080
133
MCN007 Meconium Aspiration Syndrome 51 0.080
134
c TRC078 Trichohepatoenteric Syndrome 2 31 0.080
135
P AST007 Astrocytoma 65 0.080
136
P GNT008 Giant Cell Tumor 49 0.080
137
P MMB011 Membranous Nephropathy 56 0.080
138
P MSC033 Muscle Disorders 52 0.079
139
AND005 Androgen Insensitivity Syndrome, Mild 16 0.079
140
OVR063 Overnutrition 49 0.079
141
SPS057 Spasticity 42 0.079
142
HYP005 Hypokalemia 51 0.078
143
PRP080 Peripheral Artery Disease 36 0.077
144
BNM008 Bone Mineral Density, Low 19 0.077
145
ADR009 Adrenal Cortex Disease 41 0.076
146
P GST044 Gastritis 58 0.076
147
DWR001 Dwarfism 46 0.076
148
CNS004 Constipation 57 0.076
149
ZLL002 Zollinger-Ellison Syndrome 47 0.076
150
PHR003 Pharyngitis 58 0.075
151
PNC034 Pancreas Disease 57 0.074
152
c PNC106 Pancreatic Agenesis 1 40 0.074
153
THR004 Thrombocytosis 55 0.072
154
VSC006 Vascular Cancer 54 0.072
155
P PLY019 Polyneuropathy 54 0.072
156
P VNS003 Venous Insufficiency 53 0.071
157
PLM033 Pulmonary Embolism 59 0.071
158
P OST005 Osteogenesis Imperfecta 67 0.071
159
HPT074 Hepatic Adenoma, Somatic 51 0.071
160
MRB003 Morbid Obesity 58 0.071
161
GLC003 Glucose Intolerance 55 0.070
162
GST019 Gastrointestinal Stromal Tumor 72 0.070
163
ACR007 Acromegaly 65 0.070
164
PLM010 Pulmonary Edema 56 0.069
165
GST030 Gastrinoma 41 0.069
166
FBR054 Fibroma 43 0.069
167
ART017 Aortic Disease 58 0.069
168
PRT014 Protein S Deficiency 52 0.068
169
SKL017 Skeletal Dysplasias 45 0.068
170
SKL014 Skeletal Dysplasia 46 0.068
171
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.067
172
INS001 Insulinoma 59 0.067
173
CRB025 Carbohydrate Metabolic Disorder 47 0.067
174
c ACT071 Acute Kidney Failure 50 0.066
175
P MYT002 Myotonic Dystrophy 47 0.065
176
CTS003 Coats Disease 57 0.065
177
P TRC086 Trichohepatoenteric Syndrome 1 46 0.065
178
P PYL005 Pyelonephritis 52 0.065
179
P BPL003 Bipolar Disorder 62 0.065
180
URT039 Urticaria 59 0.065
181
MYX004 Myxedema 38 0.065
182
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.064
183
P HRT017 Heart Tumor 35 0.064
184
HRT007 Heart Cancer 50 0.063
185
FBR009 Fibrous Dysplasia 44 0.063
186
CHL004 Cholelithiasis 48 0.063
187
P HYP192 Hypocalcemia, Autosomal Dominant 55 0.063
188
P TRN020 Turner Syndrome 64 0.062
189
VSC047 Vascular Malformation 45 0.062
190
PSR001 Psoriatic Arthritis 64 0.062
191
BNN003 Bone Inflammation Disease 46 0.061
192
P SPN052 Spondyloarthropathy 60 0.061
193
P DDN001 Duodenal Ulcer 51 0.061
194
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.061
195
PRP016 Paraplegia 49 0.061
196
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.060
197
HMN009 Hemangioblastoma 45 0.060
198
P PRC031 Preeclampsia/eclampsia 1 57 0.060
199
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.059
200
PPL022 Papilloma 55 0.059
201
P ALX003 Alexander Disease 64 0.059
202
P CSH001 Cushing's Syndrome 64 0.058
203
ARC002 Arachnoiditis 38 0.058
204
c HMG001 Hemoglobin C Disease 47 0.058
205
c CHR096 Chronic Pulmonary Heart Disease 40 0.057
206
APR001 Apraxia 48 0.057
207
GST023 Gastric Ulcer 55 0.057
208
P ACT080 Acute Pulmonary Heart Disease 32 0.056
209
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.056
210
P PRC019 Precocious Puberty 51 0.056
211
IMP004 Impetigo 42 0.056
212
LCT002 Lactose Intolerance 45 0.056
213
LMB062 Limb Ischemia 48 0.055
214
PRN011 Pernicious Anemia 46 0.055
215
THY030 Thyroid Gland Disease 51 0.055
216
PHS001 Phosphorus Metabolism Disease 42 0.055
217
c NRF018 Neurofibromatosis, Type 1 68 0.055
218
P ART034 Aortopulmonary Window 23 0.055
219
LRY017 Laryngeal Disease 37 0.055
220
ADR005 Adrenal Carcinoma 56 0.054
221
P ATR005 Atrophic Gastritis 45 0.054
222
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.054
223
ALX002 Alexithymia 37 0.053
224
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.053
225
P ART084 Arteriovenous Fistula 44 0.053
226
RNL078 Renal Dysplasia 45 0.053
227
VTM002 Vitamin B12 Deficiency 44 0.053
228
END038 Endocrine Pancreas Disease 43 0.052
229
ISL001 Islet Cell Tumor 50 0.052
230
LPT001 Leptospirosis 63 0.052
231
RNL097 Renal Artery Disease 45 0.052
232
NRT004 Neuritis 52 0.052
233
HYP068 Hyperostosis 40 0.050
234
CYS039 Cystic Kidney Disease 52 0.049
235
c BRN108 Branchiootic Syndrome 1 36 0.049
236
PMS001 Poems Syndrome 55 0.049
237
VSC044 Visceral Myopathy 51 0.049
238
ARC007 Arachnoid Cysts 38 0.048
239
c HMG004 Hemoglobin D Disease 33 0.048
240
SPS019 Spastic Paraparesis 34 0.048
241
KLN001 Klinefelter's Syndrome 55 0.047
242
c FML303 Familial/multiple Cancer 16 0.047
243
GLC036 Glucagonoma 40 0.047
244
ABL002 Ablepharon-Macrostomia Syndrome 57 0.047
245
P CPL003 Capillary Leak Syndrome 43 0.047
246
PLY125 Polycythemia Vera, Somatic 63 0.047
247
HYP037 Hyperhomocysteinemia 50 0.046
248
ESN011 Eisenmenger Syndrome 44 0.046
249
CYS013 Cystinuria 63 0.045
250
P ACT150 Acute Adrenal Insufficiency 45 0.045
251
P MYM002 Moyamoya Disease 60 0.045
252
MLG108 Malignant Melanoma, Somatic 67 0.045
253
PTT009 Pituitary Gland Disease 48 0.044
254
LWS003 Lowe Syndrome 61 0.043
255
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.043
256
P ATX010 Ataxia Neuropathy Spectrum 28 0.043
257
P BRC006 Brachydactyly 52 0.043
258
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.043
259
P DYS007 Dyskeratosis Congenita 63 0.042
260
SCL022 Scleredema 25 0.042
261
RNL077 Renal Fibrosis 47 0.042
262
TRN015 Transient Cerebral Ischemia 56 0.041
263
c SRC025 Sarcoidosis 1 58 0.041
264
c VRL007 Viral Encephalitis 54 0.041
265
CHY002 Chylomicron Retention Disease 59 0.041
266
P MNC007 Monocytic Leukemia 55 0.041
267
ALK013 Alkaptonuria 55 0.041
268
PTT037 Pituitary Tumors 45 0.041
269
CYS010 Cystinosis 51 0.040
270
EXT034 Extrinsic Allergic Alveolitis 56 0.040
271
PNC053 Pancreatic Islet Cell Tumors 37 0.040
272
RLP001 Relapsing Polychondritis 49 0.040
273
P PNM006 Pneumoconiosis 51 0.040
274
DNG001 Dengue Shock Syndrome 43 0.039
275
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.039
276
CRV030 Cervical Adenitis 31 0.039
277
c GRV008 Graves Disease 1 45 0.038
278
CRR007 Cirrhosis, Cryptogenic 44 0.038
279
c GLL024 Gallbladder Disease 1 38 0.037
280
EXT033 Extrapulmonary Tuberculosis 44 0.036
281
PTT008 Pituitary Carcinoma 44 0.035
282
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 25 0.035
283
CMP052 Complication in Hemodialysis 16 0.032
284
CND006 Candida Glabrata 34 0.032
285
c LNG044 Long Qt Syndrome 1 67 0.032
286
P TRC072 Treacher Collins Syndrome 1 52 0.032
287
JJN008 Jejunoileitis 37 0.031