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"

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

# Family MCID Name MIFTS Score
1
HYP315 Hyperparathyroidism, Neonatal 28 6.988
2
P HYP069 Hyperparathyroidism 57 0.933
3
c PRM005 Primary Hyperparathyroidism 56 0.700
4
P HYP004 Hypercalcemia 54 0.292
5
P HPT021 Hepatitis 74 0.285
6
ADN018 Adenoma 59 0.275
7
P THY032 Thyroiditis 57 0.272
8
P PNC044 Pancreatitis 62 0.250
9
P KDN018 Kidney Disease 64 0.244
10
P HYP086 Hypothyroidism 63 0.236
11
PRT029 Parathyroid Adenoma 46 0.222
12
PRT030 Parathyroid Gland Disease 49 0.215
13
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.207
14
END072 Endotheliitis 41 0.202
15
P ART022 Arthritis 73 0.198
16
NRN002 Neuronitis 40 0.196
17
P LKM002 Leukemia 70 0.191
18
P THR014 Thrombocytopenia 63 0.190
19
P BRS047 Breast Cancer 100 0.189
20
PRT036 Peritonitis 65 0.185
21
NTR005 Nutritional Deficiency Disease 51 0.183
22
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.179
23
P OBS005 Obesity 91 0.176
24
BNS002 Bone Structure Disease 37 0.176
25
IMP003 Impaired Renal Function Disease 36 0.166
26
P LPS004 Lupus Erythematosus 63 0.163
27
P CRV039 Cervicitis 45 0.163
28
ALR002 Al-Raqad Syndrome 36 0.160
29
c CNG401 Congenital Heart Disease 67 0.159
30
c CHR089 Chronic Kidney Failure 67 0.158
31
MLN008 Melanoma 61 0.158
32
P ADN016 Adenocarcinoma 69 0.157
33
P FML068 Familial Hypocalciuric Hypercalcemia 37 0.157
34
P URF003 Urofacial Syndrome 1 51 0.157
35
MDS022 Mediastinitis 37 0.153
36
ACD009 Acid-Labile Subunit, Deficiency of 37 0.148
37
P MYP004 Myopathy 67 0.148
38
c ACT027 Acute Pancreatitis 59 0.147
39
P RHM011 Rheumatoid Arthritis 87 0.144
40
P RCK004 Rickets 59 0.143
41
P HYP065 Hyperaldosteronism 52 0.143
42
MTH009 Mouth Disease 63 0.138
43
P HYP076 Hyperthyroidism 59 0.138
44
P MYL005 Myelofibrosis 67 0.137
45
CLT003 Colitis 56 0.137
46
ADJ001 Adjustment Disorder 38 0.136
47
c SYS001 Systemic Lupus Erythematosus 87 0.131
48
END030 End Stage Renal Failure 53 0.131
49
P AMY004 Amyloidosis 63 0.130
50
PRS047 Prostatitis 56 0.130
51
P MYC007 Myocardial Infarction 80 0.130
52
P PNC001 Pancytopenia 53 0.130
53
CYS001 Cystic Fibrosis 87 0.129
54
P HYP024 Hypoparathyroidism 52 0.129
55
MRC001 Marchiafava Bignami Disease 33 0.128
56
NPH003 Nephrocalcinosis 47 0.127
57
DDN006 Duodenitis 44 0.127
58
ACR041 Acromelic Frontonasal Dysostosis 45 0.126
59
PHY002 Physical Disorder 43 0.125
60
BRT030 Birth Defects 44 0.125
61
c PND001 Pain Disorder 53 0.124
62
END035 Endocrine Gland Cancer 50 0.121
63
GTR002 Goiter 54 0.121
64
c HPT016 Hepatitis B 61 0.121
65
CLC007 Calcium Metabolism Disease 39 0.117
66
TBR010 Tuberculosis 70 0.116
67
RNL007 Renal Tubular Acidosis 50 0.116
68
P NRV007 Nervous System Disease 71 0.114
69
P CNJ013 Conjunctivitis 65 0.113
70
P DRR001 Diarrhea 60 0.112
71
LVR012 Liver Cirrhosis 71 0.112
72
CNG034 Congestive Heart Failure 72 0.111
73
PCK002 Pick Disease 66 0.110
74
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.110
75
HYP025 Hyperphosphatemia 45 0.110
76
P SPS003 Spastic Diplegia 49 0.110
77
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.109
78
GST050 Gastrointestinal System Disease 58 0.109
79
P LRY019 Laryngitis 55 0.109
80
MTB004 Metabolic Acidosis 49 0.108
81
VND001 Vein Disease 51 0.108
82
VGN023 Vaginitis 41 0.108
83
P APL001 Aplastic Anemia 74 0.108
84
P DBT005 Diabetes Insipidus 53 0.107
85
c MLT136 Multiple Endocrine Neoplasia 1 68 0.105
86
BNF002 Bone Fracture 46 0.105
87
URM002 Uremia 36 0.105
88
GRW007 Growth Hormone Deficiency 49 0.105
89
CLC006 Calcinosis 48 0.104
90
P PHC003 Pheochromocytoma 72 0.103
91
ANX002 Anxiety Disorder 67 0.103
92
P PLY018 Polycythemia 58 0.103
93
c HPT001 Hepatitis C 68 0.103
94
ATH003 Atherosclerosis 63 0.102
95
ART021 Arteriosclerosis 59 0.102
96
P GLM007 Glomerulonephritis 56 0.101
97
ALL026 Allergic Hypersensitivity Disease 53 0.101
98
SCK005 Sickle Cell Disease 51 0.100
99
CHR005 Chorioamnionitis 47 0.099
100
c INF071 Inflammatory Bowel Disease 1 51 0.099
101
P GRV001 Graves' Disease 62 0.098
102
SPS057 Spasticity 41 0.097
103
P HMN010 Hemangioma 62 0.097
104
P PSD015 Pseudohypoparathyroidism 43 0.097
105
KRT002 Keratomalacia 50 0.096
106
P CHR345 Chronic Pain 45 0.096
107
NSD001 Nose Disease 51 0.095
108
P GST044 Gastritis 64 0.095
109
HPT074 Hepatic Adenoma, Somatic 35 0.095
110
VTM003 Vitamin Metabolic Disorder 31 0.095
111
P AST007 Astrocytoma 66 0.093
112
GLC008 Glucose Metabolism Disease 44 0.093
113
P CLC005 Celiac Disease 67 0.091
114
HDN002 Head Injury 47 0.091
115
P NPH009 Nephrolithiasis 59 0.091
116
P HYP060 Hyperinsulinism 58 0.091
117
MNR003 Mineral Metabolism Disease 39 0.091
118
MCN007 Meconium Aspiration Syndrome 52 0.090
119
IMM102 Immunodeficiency 14 33 0.090
120
P FNC004 Fanconi Syndrome 54 0.090
121
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.090
122
PHR003 Pharyngitis 58 0.090
123
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.090
124
P NRV006 Nervous System Cancer 62 0.090
125
P NRF002 Neurofibromatosis 66 0.089
126
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.089
127
P GNT008 Giant Cell Tumor 51 0.089
128
ALP008 Alopecia 56 0.089
129
ACQ007 Acquired Immunodeficiency Syndrome 60 0.088
130
P LNG028 Long Qt Syndrome 67 0.088
131
STM006 Stomach Disease 48 0.087
132
GLC003 Glucose Intolerance 56 0.087
133
ZLL002 Zollinger-Ellison Syndrome 49 0.086
134
BNM001 Bone Marrow Cancer 56 0.086
135
CNS004 Constipation 57 0.086
136
LPD004 Lipoid Nephrosis 49 0.086
137
P TBR001 Tuberous Sclerosis 68 0.085
138
HYP005 Hypokalemia 52 0.085
139
PLM033 Pulmonary Embolism 59 0.085
140
ACR007 Acromegaly 66 0.083
141
CRD137 Cardiogenic Shock 44 0.083
142
DWR001 Dwarfism 42 0.082
143
LPD008 Lipid Metabolism Disorder 42 0.082
144
PRP080 Peripheral Artery Disease 35 0.081
145
P HYP035 Hypophosphatasia 56 0.081
146
INS001 Insulinoma 60 0.080
147
MRB003 Morbid Obesity 59 0.079
148
P MMB011 Membranous Nephropathy 53 0.079
149
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.079
150
OVR063 Overnutrition 49 0.078
151
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.078
152
SPC003 Specific Developmental Disorder 39 0.078
153
FBR054 Fibroma 44 0.078
154
URN009 Urinary System Disease 52 0.078
155
c TRC078 Trichohepatoenteric Syndrome 2 30 0.078
156
P SPN052 Spondyloarthropathy 58 0.078
157
BNN003 Bone Inflammation Disease 46 0.077
158
P DDN001 Duodenal Ulcer 51 0.077
159
MYX004 Myxedema 36 0.077
160
P PLY019 Polyneuropathy 53 0.076
161
P OST005 Osteogenesis Imperfecta 68 0.076
162
CHL004 Cholelithiasis 48 0.076
163
ACR002 Acrocapitofemoral Dysplasia 35 0.075
164
BNM008 Bone Mineral Density, Low 28 0.075
165
BND014 Bone Development Disease 40 0.075
166
PLS007 Plasmodium Falciparum Malaria 56 0.075
167
GST030 Gastrinoma 39 0.075
168
GST019 Gastrointestinal Stromal Tumor 73 0.075
169
FBR009 Fibrous Dysplasia 44 0.075
170
PLM010 Pulmonary Edema 56 0.075
171
PRP016 Paraplegia 49 0.074
172
PRT014 Protein S Deficiency 54 0.073
173
MSC004 Muscle Tissue Disease 35 0.073
174
HMN009 Hemangioblastoma 45 0.073
175
SKL014 Skeletal Dysplasia 44 0.073
176
SKL017 Skeletal Dysplasias 41 0.073
177
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.073
178
PPL022 Papilloma 54 0.072
179
P MSC033 Muscle Disorders 52 0.072
180
P PYL005 Pyelonephritis 52 0.071
181
P VNS003 Venous Insufficiency 53 0.071
182
PRN011 Pernicious Anemia 41 0.071
183
P ATR005 Atrophic Gastritis 47 0.071
184
P MYT002 Myotonic Dystrophy 46 0.071
185
ADR009 Adrenal Cortex Disease 40 0.071
186
VSC006 Vascular Cancer 51 0.070
187
P ART034 Aortopulmonary Window 23 0.069
188
c NRF018 Neurofibromatosis, Type 1 69 0.069
189
ADR005 Adrenal Carcinoma 57 0.069
190
P TRN020 Turner Syndrome 64 0.068
191
TCL003 T Cell Deficiency 44 0.068
192
ART017 Aortic Disease 57 0.067
193
PSR001 Psoriatic Arthritis 64 0.066
194
ADR008 Adrenal Adenoma 49 0.066
195
P TRC086 Trichohepatoenteric Syndrome 1 46 0.066
196
P PRC031 Preeclampsia/eclampsia 1 53 0.066
197
CRB025 Carbohydrate Metabolic Disorder 46 0.065
198
GST023 Gastric Ulcer 56 0.065
199
c ACT071 Acute Kidney Failure 48 0.065
200
VHW001 Vohwinkel Syndrome 47 0.065
201
CYS039 Cystic Kidney Disease 49 0.065
202
ARC002 Arachnoiditis 38 0.064
203
LPT001 Leptospirosis 65 0.064
204
CTS003 Coats Disease 57 0.064
205
SPS019 Spastic Paraparesis 34 0.064
206
APR001 Apraxia 50 0.063
207
HPY002 H. Pylori Infection 58 0.063
208
P PRC019 Precocious Puberty 53 0.063
209
ABL002 Ablepharon-Macrostomia Syndrome 51 0.063
210
GLC036 Glucagonoma 47 0.063
211
IMP004 Impetigo 41 0.062
212
VSC047 Vascular Malformation 45 0.062
213
P HYP192 Hypocalcemia, Autosomal Dominant 50 0.062
214
OTP003 Oto-Palatal-Digital Syndrome 14 0.061
215
NRT004 Neuritis 52 0.061
216
c GRV008 Graves Disease 1 44 0.061
217
CYS013 Cystinuria 63 0.060
218
SLV003 Salivary Gland Disease 47 0.060
219
ALX002 Alexithymia 37 0.060
220
P DGR001 Digeorge Syndrome 52 0.060
221
CMB003 Combined T Cell and B Cell Immunodeficiency 46 0.060
222
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.059
223
LCT002 Lactose Intolerance 45 0.059
224
DMY004 Demyelinating Disease 52 0.059
225
ISL001 Islet Cell Tumor 51 0.059
226
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.059
227
CHR078 Chorioretinitis 41 0.058
228
c HMG001 Hemoglobin C Disease 46 0.058
229
SCL022 Scleredema 27 0.058
230
RNL078 Renal Dysplasia 48 0.057
231
VNT001 Ventilation Pneumonitis 35 0.057
232
PMS001 Poems Syndrome 56 0.057
233
c BRN108 Branchiootic Syndrome 1 36 0.057
234
c CHR096 Chronic Pulmonary Heart Disease 40 0.057
235
c ATM060 Autoimmune Atrophic Gastritis 18 0.056
236
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 25 0.056
237
P ACT080 Acute Pulmonary Heart Disease 31 0.055
238
ALK013 Alkaptonuria 54 0.055
239
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.055
240
HYP068 Hyperostosis 39 0.054
241
P TRC072 Treacher Collins Syndrome 1 50 0.054
242
LRY017 Laryngeal Disease 33 0.054
243
ARC007 Arachnoid Cysts 39 0.054
244
THY030 Thyroid Gland Disease 52 0.053
245
P DYS007 Dyskeratosis Congenita 64 0.053
246
RNL097 Renal Artery Disease 44 0.052
247
c SCN036 Secondary Progressive Multiple Sclerosis 50 0.052
248
P ART084 Arteriovenous Fistula 40 0.052
249
VTM002 Vitamin B12 Deficiency 45 0.051
250
EXT034 Extrinsic Allergic Alveolitis 58 0.051
251
PHS001 Phosphorus Metabolism Disease 39 0.051
252
ESN011 Eisenmenger Syndrome 45 0.050
253
CST005 Castleman Disease 42 0.050
254
P BRC006 Brachydactyly 53 0.050
255
P MYM002 Moyamoya Disease 60 0.050
256
P ACT150 Acute Adrenal Insufficiency 36 0.050
257
INT040 Intrinsic Asthma 40 0.050
258
P PNM006 Pneumoconiosis 51 0.049
259
HYR002 Hoyeraal Hreidarsson Syndrome 37 0.049
260
TWN003 Townes-Brocks Syndrome 55 0.048
261
DNG001 Dengue Shock Syndrome 41 0.048
262
PNC053 Pancreatic Islet Cell Tumors 37 0.048
263
VSC044 Visceral Myopathy 44 0.048
264
TRN015 Transient Cerebral Ischemia 57 0.048
265
c HMG004 Hemoglobin D Disease 32 0.047
266
KLN001 Klinefelter's Syndrome 52 0.047
267
c FML303 Familial/multiple Cancer 15 0.047
268
EXT033 Extrapulmonary Tuberculosis 45 0.046
269
RNL077 Renal Fibrosis 48 0.046
270
c PNC108 Pancreatitis, Hereditary 59 0.046
271
CRV030 Cervical Adenitis 30 0.046
272
PTT009 Pituitary Gland Disease 45 0.045
273
CYS010 Cystinosis 51 0.045
274
ENC003 Encephalitozoonosis 31 0.044
275
LWS003 Lowe Syndrome 61 0.043
276
c SRC025 Sarcoidosis 1 58 0.043
277
CRY001 Cryptogenic Organizing Pneumonia 44 0.043
278
P MDL022 Medullary Thyroid Carcinoma, Familial 62 0.042
279
P GCH001 Gaucher's Disease 63 0.042
280
c ART106 Arterial Calcification, Generalized, of Infancy, 1 32 0.041
281
JJN008 Jejunoileitis 38 0.040
282
CND006 Candida Glabrata 35 0.040
283
PTT037 Pituitary Tumors 45 0.039
284
PTT008 Pituitary Carcinoma 45 0.038
285
CMP052 Complication in Hemodialysis 14 0.032