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disorder_subdivision.id | disorder_subdivision.ts | disorder_subdivision.value |
---|---|---|
1 | 2017-09-20 04:38:45 | None |
11 | 2017-09-20 04:39:27 | familial amyloidosis |
12 | 2017-09-20 04:39:27 | primary amyloidosis |
13 | 2017-09-20 04:39:27 | secondary amyloidosis |
14 | 2017-09-20 04:39:27 | senile amyloidosis |
16 | 2017-09-20 04:39:39 | congenital fibrosis of the extraocular muscles 2 (CFEOM 2) |
17 | 2017-09-20 04:39:39 | congenital fibrosis of the extraocular muscles 3 (CFEOM 3) |
18 | 2017-09-20 04:39:39 | Tukel syndrome |
19 | 2017-09-20 04:39:39 | congenital fibrosis of the extraocular muscles 1 (CFEOM 1) |
23 | 2017-09-20 04:40:45 | Multisynostotic Osteodysgenesis |
32 | 2017-09-20 04:42:18 | epidermolysis bullosa simplex |
33 | 2017-09-20 04:42:18 | junctional epidermolysis bullosa |
34 | 2017-09-20 04:42:18 | dystrophic epidermolysis bullosa |
35 | 2017-09-20 04:42:18 | Kindler syndrome |
42 | 2017-09-20 04:42:33 | Autosomal Recessive Inheritance ACC (e.g. Andermann syndrome) |
43 | 2017-09-20 04:42:33 | X-Linked Dominant Inheritance ACC (e.g. ARX) |
44 | 2017-09-20 04:42:33 | Acquired Form of ACC |
45 | 2017-09-20 04:42:33 | Aicardi Syndrome |
61 | 2017-09-20 04:44:05 | infantile onset Pompe disease |
62 | 2017-09-20 04:44:05 | late onset Pompe disease |
65 | 2017-09-20 04:44:24 | Propionic Acidemia, Type I (PCCA Deficiency) |
66 | 2017-09-20 04:44:24 | Propionic Acidemia, Type II (PCCB Deficiency) |
70 | 2017-09-20 04:45:48 | X-linked agammaglobulinemia (XLA) |
71 | 2017-09-20 04:45:48 | X-linked agammaglobulinemia with growth hormone deficiency |
72 | 2017-09-20 04:45:48 | autosomal recessive agammaglobulinemia |
88 | 2017-09-20 04:47:19 | subcortical band heterotopia |
89 | 2017-09-20 04:47:19 | Miller-Dieker syndrome |
90 | 2017-09-20 04:47:19 | Norman-Roberts syndrome |
91 | 2017-09-20 04:47:19 | isolated lissencephaly sequence (ILS) |
92 | 2017-09-20 04:47:19 | lissencephaly 1 (LIS1) |
93 | 2017-09-20 04:47:19 | x-linked lissencephaly |
105 | 2017-09-20 04:48:43 | Osteopetrosis, autosomal recessive; malignant infantile type |
106 | 2017-09-20 04:48:43 | Osteopetrosis, autosomal dominant; adult type |
107 | 2017-09-20 04:48:43 | Osteopetrosis, mild autosomal recessive; intermediate type |
108 | 2017-09-20 04:48:45 | oculocutaneous albinism type 1A |
109 | 2017-09-20 04:48:45 | oculocutaneous albinism type 1B |
110 | 2017-09-20 04:48:45 | oculocutaneous albinism type 2 |
111 | 2017-09-20 04:48:45 | oculocutaneous albinism type 3 |
112 | 2017-09-20 04:48:45 | oculocutaneous albinism type 4 |
136 | 2017-09-20 04:52:32 | Alopecia Universalis |
137 | 2017-09-20 04:52:32 | Alopecia Totalis |
138 | 2017-09-20 04:52:32 | Alopecia Seminuniversalis |
150 | 2017-09-20 04:53:19 | classical |
151 | 2017-09-20 04:53:19 | later-onset |
152 | 2017-09-20 04:53:21 | Kanzaki disease |
153 | 2017-09-20 04:53:21 | Schindler disease Type I |
154 | 2017-09-20 04:53:21 | Schindler disease Type II |
155 | 2017-09-20 04:53:21 | Schindler disease Type III |
160 | 2017-09-20 04:53:31 | fucosidosis type 1 |
161 | 2017-09-20 04:53:31 | fucosidosis type 2 |
163 | 2017-09-20 04:53:41 | alpha-mannosidosis, type I |
164 | 2017-09-20 04:53:41 | alpha-mannosidosis, type II |
165 | 2017-09-20 04:53:41 | alpha-mannosidosis, type III |
174 | 2017-09-20 04:54:58 | Central Apnea |
175 | 2017-09-20 04:54:58 | Diaphragmatic Apnea |
176 | 2017-09-20 04:54:58 | Obstructive Apnea |
177 | 2017-09-20 04:54:58 | Upper Airway Apnea |
178 | 2017-09-20 04:54:58 | Mixed Apnea |
186 | 2017-09-20 04:55:17 | Apraxia, Oculomotor |
187 | 2017-09-20 04:55:17 | Apraxia, Classic |
188 | 2017-09-20 04:55:17 | Apraxia, Ideokinetic |
189 | 2017-09-20 04:55:17 | Apraxia, Ideomotor |
190 | 2017-09-20 04:55:17 | Apraxia, Motor |
191 | 2017-09-20 04:55:17 | Apraxia, Ideational |
192 | 2017-09-20 04:55:17 | Apraxia, Buccofacial |
193 | 2017-09-20 04:55:17 | Apraxia, Constructional |
194 | 2017-09-20 04:55:32 | adhesive arachnoiditis |
195 | 2017-09-20 04:55:32 | arachnoiditis ossificans |
196 | 2017-09-20 04:55:32 | hereditary arachnoiditis |
197 | 2017-09-20 04:55:32 | neoplastic arachnoiditis |
198 | 2017-09-20 04:55:32 | optochiasmatic arachnoiditis |
199 | 2017-09-20 04:55:32 | postmyelographic arachnoiditis |
200 | 2017-09-20 04:55:32 | rhinosinusogenic cerebral arachnoiditis |
201 | 2017-09-20 04:55:32 | cerebral arachnoiditis |
202 | 2017-09-20 04:55:32 | Marfan syndrome type I |
203 | 2017-09-20 04:55:32 | Marfan syndrome type II |
205 | 2017-09-20 04:55:44 | intracranial arachnoid cysts |
206 | 2017-09-20 04:55:44 | spinal arachnoid cysts |
207 | 2017-09-20 04:55:48 | Frontal Tumor, Meningioma |
208 | 2017-09-20 04:55:48 | Temporal Tumor, Meningioma |
209 | 2017-09-20 04:55:48 | Parietal Tumor, Meningioma |
221 | 2017-09-20 04:56:51 | familial Mediterranean fever type 1 |
222 | 2017-09-20 04:56:51 | familial Mediterranean fever type 2 |
224 | 2017-09-20 04:57:27 | Late Infantile Metachromatic Leukodystrophy |
225 | 2017-09-20 04:57:27 | Juvenile Metachromatic Leukodystrophy |
226 | 2017-09-20 04:57:27 | Adult Metachromatic Leukodystrophy |
228 | 2017-09-20 04:57:45 | arteriovenous malformation of the brain |
229 | 2017-09-20 04:57:45 | arteriovenous malformation of the spine |
234 | 2017-09-20 04:59:34 | Aquagenic Urticaria |
235 | 2017-09-20 04:59:34 | Cold Urticaria |
236 | 2017-09-20 04:59:34 | Dermatographia |
237 | 2017-09-20 04:59:34 | Dermographism |
248 | 2017-09-20 05:01:15 | Complete Atrioventricular Septal Defect |
249 | 2017-09-20 05:01:15 | Transitional Atrioventricular Septal Defect |
250 | 2017-09-20 05:01:15 | Incomplete Atrioventricular Septal Defect |
251 | 2017-09-20 05:01:15 | Partial Atrioventricular Septal Defect |
253 | 2017-09-20 05:01:31 | Machado-Joseph Disease Type I (MJD-I) |
254 | 2017-09-20 05:01:31 | Machado-Joseph Disease Type II (MJD-II) |
255 | 2017-09-20 05:01:31 | Machado-Joseph Disease Type III (MJD-III) |
270 | 2017-09-20 05:04:05 | Acute Brucellosis |
disorder_subdivision.id | disorder_subdivision.ts | disorder_subdivision.value |