achraf2203/pfe-raredisease
03
1{
2 "nodes": [
3 {
4 "id": "C0678236",
5 "name": "Rare Diseases",
6 "type": "Disease",
7 "source": "UMLS"
8 },
9 {
10 "id": "C1834219",
11 "name": "Parathyroid disease rare",
12 "type": "Disease",
13 "source": "UMLS"
14 },
15 {
16 "id": "C0920627",
17 "name": "Orphan Diseases",
18 "type": "Disease",
19 "source": "UMLS"
20 },
21 {
22 "id": "C0019247",
23 "name": "Hereditary Diseases",
24 "type": "Disease",
25 "source": "UMLS"
26 },
27 {
28 "id": "C5816793",
29 "name": "Imprinting Disorders",
30 "type": "Disease",
31 "source": "UMLS"
32 },
33 {
34 "id": "C0013720",
35 "name": "Ehlers-Danlos Syndrome",
36 "type": "Disease",
37 "source": "UMLS"
38 },
39 {
40 "id": "C0268344",
41 "name": "Ehlers-Danlos syndrome 6B",
42 "type": "Disease",
43 "source": "UMLS"
44 },
45 {
46 "id": "C0268338",
47 "name": "Ehlers-Danlos Syndrome, Type IV",
48 "type": "Disease",
49 "source": "UMLS"
50 },
51 {
52 "id": "C0268342",
53 "name": "Ehlers-Danlos syndrome type 6",
54 "type": "Disease",
55 "source": "UMLS"
56 },
57 {
58 "id": "C0268336",
59 "name": "Ehlers-Danlos syndrome type 2",
60 "type": "Disease",
61 "source": "UMLS"
62 },
63 {
64 "id": "C0268335",
65 "name": "Ehlers-Danlos syndrome type 1",
66 "type": "Disease",
67 "source": "UMLS"
68 },
69 {
70 "id": "C0268347",
71 "name": "Ehlers-Danlos Syndrome, Type VIII",
72 "type": "Disease",
73 "source": "UMLS"
74 },
75 {
76 "id": "C0268337",
77 "name": "Ehlers-Danlos syndrome, type 3 (disorder)",
78 "type": "Disease",
79 "source": "UMLS"
80 },
81 {
82 "id": "C0268341",
83 "name": "Ehlers-Danlos syndrome type 5",
84 "type": "Disease",
85 "source": "UMLS"
86 },
87 {
88 "id": "C4552003",
89 "name": "Ehlers-Danlos syndrome progeroid type",
90 "type": "Disease",
91 "source": "UMLS"
92 },
93 {
94 "id": "C2676510",
95 "name": "Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like",
96 "type": "Disease",
97 "source": "UMLS"
98 },
99 {
100 "id": "C4551497",
101 "name": "Ehlers-Danlos syndrome kyphoscoliotic type",
102 "type": "Disease",
103 "source": "UMLS"
104 },
105 {
106 "id": "C1857034",
107 "name": "Ehlers-Danlos syndrome, cardiac valvular form",
108 "type": "Disease",
109 "source": "UMLS"
110 },
111 {
112 "id": "C2700425",
113 "name": "EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE",
114 "type": "Disease",
115 "source": "UMLS"
116 },
117 {
118 "id": "C1857038",
119 "name": "Ehlers-Danlos Syndrome with Platelet Dysfunction from Fibronectin Abnormality",
120 "type": "Disease",
121 "source": "UMLS"
122 },
123 {
124 "id": "C4225429",
125 "name": "Ehlers-Danlos syndrome classic type",
126 "type": "Disease",
127 "source": "UMLS"
128 },
129 {
130 "id": "C1837462",
131 "name": "Ehlers-Danlos syndrome, Beasley Cohen type",
132 "type": "Disease",
133 "source": "UMLS"
134 },
135 {
136 "id": "C4551623",
137 "name": "EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1",
138 "type": "Disease",
139 "source": "UMLS"
140 },
141 {
142 "id": "C0220679",
143 "name": "Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified",
144 "type": "Disease",
145 "source": "UMLS"
146 },
147 {
148 "id": "C1848029",
149 "name": "Ehlers-Danlos syndrome caused by tenascin-X deficiency",
150 "type": "Disease",
151 "source": "UMLS"
152 },
153 {
154 "id": "C1866294",
155 "name": "EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1",
156 "type": "Disease",
157 "source": "UMLS"
158 },
159 {
160 "id": "C3502156",
161 "name": "Ehlers-Danlos Syndrome VI Phenotype with Macrocephaly",
162 "type": "Disease",
163 "source": "UMLS"
164 },
165 {
166 "id": "C4303789",
167 "name": "Ehlers-Danlos syndrome cardiac valvular type",
168 "type": "Disease",
169 "source": "UMLS"
170 },
171 {
172 "id": "C3809210",
173 "name": "B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome",
174 "type": "Disease",
175 "source": "UMLS"
176 },
177 {
178 "id": "C4540530",
179 "name": "EHLERS-DANLOS SYNDROME, NONVASCULAR VARIANT",
180 "type": "Disease",
181 "source": "UMLS"
182 },
183 {
184 "id": "C0024796",
185 "name": "Marfan Syndrome",
186 "type": "Disease",
187 "source": "UMLS"
188 },
189 {
190 "id": "C4016054",
191 "name": "Neonatal Marfan syndrome",
192 "type": "Disease",
193 "source": "UMLS"
194 },
195 {
196 "id": "C4016055",
197 "name": "MARFAN SYNDROME, ATYPICAL",
198 "type": "Disease",
199 "source": "UMLS"
200 },
201 {
202 "id": "C4016056",
203 "name": "MARFAN SYNDROME, MILD",
204 "type": "Disease",
205 "source": "UMLS"
206 },
207 {
208 "id": "C4016057",
209 "name": "MARFAN SYNDROME, CLASSIC",
210 "type": "Disease",
211 "source": "UMLS"
212 },
213 {
214 "id": "C4721845",
215 "name": "Marfan Syndrome, Type I",
216 "type": "Disease",
217 "source": "UMLS"
218 },
219 {
220 "id": "C2931058",
221 "name": "Marfan Syndrome Type 2",
222 "type": "Disease",
223 "source": "UMLS"
224 },
225 {
226 "id": "C4016053",
227 "name": "MARFAN SYNDROME, MILD VARIABLE",
228 "type": "Disease",
229 "source": "UMLS"
230 },
231 {
232 "id": "C4016052",
233 "name": "MARFAN SYNDROME, SEVERE CLASSIC",
234 "type": "Disease",
235 "source": "UMLS"
236 },
237 {
238 "id": "C4016059",
239 "name": "MARFAN SYNDROME, AUTOSOMAL RECESSIVE",
240 "type": "Disease",
241 "source": "UMLS"
242 },
243 {
244 "id": "C4310796",
245 "name": "MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME",
246 "type": "Disease",
247 "source": "UMLS"
248 },
249 {
250 "id": "C2674574",
251 "name": "Aortic aneurysm, familial thoracic 3",
252 "type": "Disease",
253 "source": "UMLS"
254 },
255 {
256 "id": "C4308213",
257 "name": "FBN1 protein, human",
258 "type": "Disease",
259 "source": "UMLS"
260 },
261 {
262 "id": "C0002986",
263 "name": "Fabry Disease",
264 "type": "Disease",
265 "source": "UMLS"
266 },
267 {
268 "id": "C1970820",
269 "name": "Fabry Disease, Cardiac Variant",
270 "type": "Disease",
271 "source": "UMLS"
272 },
273 {
274 "id": "C0017205",
275 "name": "Gaucher Disease",
276 "type": "Disease",
277 "source": "UMLS"
278 },
279 {
280 "id": "C0268251",
281 "name": "Gaucher Disease, Type 3",
282 "type": "Disease",
283 "source": "UMLS"
284 },
285 {
286 "id": "C0268250",
287 "name": "Gaucher Disease, Type 2",
288 "type": "Disease",
289 "source": "UMLS"
290 },
291 {
292 "id": "C1961835",
293 "name": "Gaucher Disease, Type 1",
294 "type": "Disease",
295 "source": "UMLS"
296 },
297 {
298 "id": "C2931585",
299 "name": "Gaucher-like disease",
300 "type": "Disease",
301 "source": "UMLS"
302 },
303 {
304 "id": "C1842704",
305 "name": "GAUCHER DISEASE, PERINATAL LETHAL",
306 "type": "Disease",
307 "source": "UMLS"
308 },
309 {
310 "id": "C1856476",
311 "name": "Gaucher Disease, Type Iiic",
312 "type": "Disease",
313 "source": "UMLS"
314 },
315 {
316 "id": "C1856491",
317 "name": "Gaucher Disease, Type IIIa",
318 "type": "Disease",
319 "source": "UMLS"
320 },
321 {
322 "id": "C1856492",
323 "name": "Gaucher Disease, Type IIIb",
324 "type": "Disease",
325 "source": "UMLS"
326 },
327 {
328 "id": "C1856493",
329 "name": "Gaucher Disease, Norrbottnian Type",
330 "type": "Disease",
331 "source": "UMLS"
332 },
333 {
334 "id": "C2930815",
335 "name": "Acute cerebral Gaucher disease",
336 "type": "Disease",
337 "source": "UMLS"
338 },
339 {
340 "id": "C1864651",
341 "name": "GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY",
342 "type": "Disease",
343 "source": "UMLS"
344 },
345 {
346 "id": "C1436561",
347 "name": "PSAP protein, human",
348 "type": "Disease",
349 "source": "UMLS"
350 },
351 {
352 "id": "C0020179",
353 "name": "Huntington Disease",
354 "type": "Disease",
355 "source": "UMLS"
356 },
357 {
358 "id": "C0751208",
359 "name": "Juvenile Huntington Disease",
360 "type": "Disease",
361 "source": "UMLS"
362 },
363 {
364 "id": "C1864112",
365 "name": "HUNTINGTON DISEASE-LIKE 1",
366 "type": "Disease",
367 "source": "UMLS"
368 },
369 {
370 "id": "C3711380",
371 "name": "Huntington Disease-Like Syndrome",
372 "type": "Disease",
373 "source": "UMLS"
374 },
375 {
376 "id": "C1847987",
377 "name": "HUNTINGTON DISEASE-LIKE 2",
378 "type": "Disease",
379 "source": "UMLS"
380 },
381 {
382 "id": "C0393574",
383 "name": "Huntington Disease, Late Onset",
384 "type": "Disease",
385 "source": "UMLS"
386 },
387 {
388 "id": "C1858114",
389 "name": "HUNTINGTON DISEASE-LIKE 3 (disorder)",
390 "type": "Disease",
391 "source": "UMLS"
392 },
393 {
394 "id": "C0751207",
395 "name": "Akinetic-Rigid Variant of Huntington Disease",
396 "type": "Disease",
397 "source": "UMLS"
398 },
399 {
400 "id": "C4255255",
401 "name": "Huntingtin Protein",
402 "type": "Disease",
403 "source": "UMLS"
404 },
405 {
406 "id": "C1846707",
407 "name": "SPINOCEREBELLAR ATAXIA 17",
408 "type": "Disease",
409 "source": "UMLS"
410 },
411 {
412 "id": "C0252274",
413 "name": "HD protein, human",
414 "type": "Disease",
415 "source": "UMLS"
416 },
417 {
418 "id": "C1675330",
419 "name": "Htt protein, mouse",
420 "type": "Disease",
421 "source": "UMLS"
422 },
423 {
424 "id": "C1567843",
425 "name": "Htt protein, rat",
426 "type": "Disease",
427 "source": "UMLS"
428 },
429 {
430 "id": "C1279186",
431 "name": "Westphal disease",
432 "type": "Disease",
433 "source": "UMLS"
434 },
435 {
436 "id": "C0010674",
437 "name": "Cystic Fibrosis",
438 "type": "Disease",
439 "source": "UMLS"
440 },
441 {
442 "id": "C0392164",
443 "name": "Pulmonary Cystic Fibrosis",
444 "type": "Disease",
445 "source": "UMLS"
446 },
447 {
448 "id": "C0056888",
449 "name": "cystic fibrosis serum factor",
450 "type": "Disease",
451 "source": "UMLS"
452 },
453 {
454 "id": "C0056889",
455 "name": "Cystic Fibrosis Transmembrane Conductance Regulator",
456 "type": "Disease",
457 "source": "UMLS"
458 },
459 {
460 "id": "C1859047",
461 "name": "CYSTIC FIBROSIS, MODIFIER OF, 1",
462 "type": "Disease",
463 "source": "UMLS"
464 },
465 {
466 "id": "C2931413",
467 "name": "Follicular hamartoma alopecia cystic fibrosis",
468 "type": "Disease",
469 "source": "UMLS"
470 },
471 {
472 "id": "C1527396",
473 "name": "Fibrocystic Disease of Pancreas",
474 "type": "Disease",
475 "source": "UMLS"
476 },
477 {
478 "id": "C4016407",
479 "name": "CYSTIC FIBROSIS LUNG DISEASE, MODIFIER OF",
480 "type": "Disease",
481 "source": "UMLS"
482 },
483 {
484 "id": "C4016791",
485 "name": "SWEAT CHLORIDE ELEVATION WITHOUT CYSTIC FIBROSIS",
486 "type": "Disease",
487 "source": "UMLS"
488 },
489 {
490 "id": "C1366582",
491 "name": "S100A8 gene",
492 "type": "Disease",
493 "source": "UMLS"
494 },
495 {
496 "id": "C0054504",
497 "name": "Calgranulin A",
498 "type": "Disease",
499 "source": "UMLS"
500 },
501 {
502 "id": "C0651197",
503 "name": "cystic fibrosis transmembrane conductance regulator (505-511)",
504 "type": "Disease",
505 "source": "UMLS"
506 },
507 {
508 "id": "C0297062",
509 "name": "cystic fibrosis transmembrane conductance regulator delta F508",
510 "type": "Disease",
511 "source": "UMLS"
512 },
513 {
514 "id": "C3276246",
515 "name": "MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO",
516 "type": "Disease",
517 "source": "UMLS"
518 },
519 {
520 "id": "C1335798",
521 "name": "S100A9 gene",
522 "type": "Disease",
523 "source": "UMLS"
524 },
525 {
526 "id": "C2749757",
527 "name": "BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1",
528 "type": "Disease",
529 "source": "UMLS"
530 },
531 {
532 "id": "C2751324",
533 "name": "BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3",
534 "type": "Disease",
535 "source": "UMLS"
536 },
537 {
538 "id": "C2751666",
539 "name": "BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2",
540 "type": "Disease",
541 "source": "UMLS"
542 },
543 {
544 "id": "C0055725",
545 "name": "ciliary dyskinesia factor",
546 "type": "Disease",
547 "source": "UMLS"
548 },
549 {
550 "id": "C1413365",
551 "name": "CFTR gene",
552 "type": "Disease",
553 "source": "UMLS"
554 },
555 {
556 "id": "C1840270",
557 "name": "PSEUDOMONAS AERUGINOSA, SUSCEPTIBILITY TO CHRONIC INFECTION BY, IN CYSTIC FIBROSIS",
558 "type": "Disease",
559 "source": "UMLS"
560 },
561 {
562 "id": "C1857424",
563 "name": "Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality",
564 "type": "Disease",
565 "source": "UMLS"
566 },
567 {
568 "id": "C3806255",
569 "name": "CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND IMPAIRED INTELLECTUAL DEVELOPMENT",
570 "type": "Disease",
571 "source": "UMLS"
572 },
573 {
574 "id": "C3659855",
575 "name": "CFTR protein, rat",
576 "type": "Disease",
577 "source": "UMLS"
578 },
579 {
580 "id": "C4742376",
581 "name": "Cftr protein, mouse",
582 "type": "Disease",
583 "source": "UMLS"
584 },
585 {
586 "id": "C0751434",
587 "name": "Classical phenylketonuria",
588 "type": "Disease",
589 "source": "UMLS"
590 },
591 {
592 "id": "C0031485",
593 "name": "Phenylketonurias",
594 "type": "Disease",
595 "source": "UMLS"
596 },
597 {
598 "id": "C0268465",
599 "name": "Phenylketonuria II",
600 "type": "Disease",
601 "source": "UMLS"
602 },
603 {
604 "id": "C0085547",
605 "name": "Phenylketonuria, Maternal",
606 "type": "Disease",
607 "source": "UMLS"
608 },
609 {
610 "id": "C0002895",
611 "name": "Anemia, Sickle Cell",
612 "type": "Disease",
613 "source": "UMLS"
614 },
615 {
616 "id": "C0019034",
617 "name": "Hemoglobin SC Disease",
618 "type": "Disease",
619 "source": "UMLS"
620 },
621 {
622 "id": "C0039730",
623 "name": "Thalassemia",
624 "type": "Disease",
625 "source": "UMLS"
626 },
627 {
628 "id": "C0005283",
629 "name": "beta Thalassemia",
630 "type": "Disease",
631 "source": "UMLS"
632 },
633 {
634 "id": "C0002312",
635 "name": "alpha-Thalassemia",
636 "type": "Disease",
637 "source": "UMLS"
638 },
639 {
640 "id": "C0085578",
641 "name": "Thalassemia Minor",
642 "type": "Disease",
643 "source": "UMLS"
644 },
645 {
646 "id": "C0271979",
647 "name": "Thalassemia Intermedia",
648 "type": "Disease",
649 "source": "UMLS"
650 },
651 {
652 "id": "C0271990",
653 "name": "delta-Thalassemia",
654 "type": "Disease",
655 "source": "UMLS"
656 },
657 {
658 "id": "C0271985",
659 "name": "Delta-Beta Thalassemia",
660 "type": "Disease",
661 "source": "UMLS"
662 },
663 {
664 "id": "C0472762",
665 "name": "Alpha trait thalassemia",
666 "type": "Disease",
667 "source": "UMLS"
668 },
669 {
670 "id": "C0472767",
671 "name": "Beta thalassemia intermedia",
672 "type": "Disease",
673 "source": "UMLS"
674 },
675 {
676 "id": "C0002875",
677 "name": "Cooley's anemia",
678 "type": "Disease",
679 "source": "UMLS"
680 },
681 {
682 "id": "C3841475",
683 "name": "Beta plus thalassemia",
684 "type": "Disease",
685 "source": "UMLS"
686 },
687 {
688 "id": "C0271980",
689 "name": "Beta zero thalassemia",
690 "type": "Disease",
691 "source": "UMLS"
692 },
693 {
694 "id": "C0271991",
695 "name": "Delta zero thalassemia",
696 "type": "Disease",
697 "source": "UMLS"
698 },
699 {
700 "id": "C1456873",
701 "name": "Alpha plus thalassemia",
702 "type": "Disease",
703 "source": "UMLS"
704 },
705 {
706 "id": "C0472777",
707 "name": "Hemoglobin E/beta thalassemia disease",
708 "type": "Disease",
709 "source": "UMLS"
710 },
711 {
712 "id": "C4016190",
713 "name": "DELTA-PLUS-THALASSEMIA",
714 "type": "Disease",
715 "source": "UMLS"
716 },
717 {
718 "id": "C4017494",
719 "name": "BETA-KNOSSOS-THALASSEMIA",
720 "type": "Disease",
721 "source": "UMLS"
722 },
723 {
724 "id": "C4017510",
725 "name": "BETA-MALAY-THALASSEMIA",
726 "type": "Disease",
727 "source": "UMLS"
728 },
729 {
730 "id": "C4017526",
731 "name": "BETA-HOUSTON-THALASSEMIA",
732 "type": "Disease",
733 "source": "UMLS"
734 },
735 {
736 "id": "C1858990",
737 "name": "Beta Thalassemia, Dominant Inclusion Body Type",
738 "type": "Disease",
739 "source": "UMLS"
740 },
741 {
742 "id": "C0585216",
743 "name": "Alpha-Thalassemia Myelodysplasia Syndrome",
744 "type": "Disease",
745 "source": "UMLS"
746 },
747 {
748 "id": "C4310973",
749 "name": "BETA-THALASSEMIA INTERMEDIA, DOMINANT",
750 "type": "Disease",
751 "source": "UMLS"
752 },
753 {
754 "id": "C4017522",
755 "name": "BETA-SHOWA-YAKUSHIJI THALASSEMIA",
756 "type": "Disease",
757 "source": "UMLS"
758 },
759 {
760 "id": "C4016247",
761 "name": "Gamma delta beta thalassemia",
762 "type": "Disease",
763 "source": "UMLS"
764 },
765 {
766 "id": "C1861232",
767 "name": "Thalassemia, Beta+, Silent Allele",
768 "type": "Disease",
769 "source": "UMLS"
770 },
771 {
772 "id": "C0019202",
773 "name": "Hepatolenticular Degeneration",
774 "type": "Disease",
775 "source": "UMLS"
776 },
777 {
778 "id": "C0296649",
779 "name": "Wilson disease protein",
780 "type": "Disease",
781 "source": "UMLS"
782 },
783 {
784 "id": "C1527352",
785 "name": "Hepatic Form of Wilson Disease",
786 "type": "Disease",
787 "source": "UMLS"
788 },
789 {
790 "id": "C4759705",
791 "name": "Intracapillary glomerulosclerosis due to diabetes mellitus",
792 "type": "Disease",
793 "source": "UMLS"
794 },
795 {
796 "id": "C4547003",
797 "name": "ATP7B protein, human",
798 "type": "Disease",
799 "source": "UMLS"
800 },
801 {
802 "id": "C0019069",
803 "name": "Hemophilia A",
804 "type": "Disease",
805 "source": "UMLS"
806 },
807 {
808 "id": "C0008533",
809 "name": "Hemophilia B",
810 "type": "Disease",
811 "source": "UMLS"
812 },
813 {
814 "id": "C5848256",
815 "name": "Hemophilia B Leyden",
816 "type": "Disease",
817 "source": "UMLS"
818 },
819 {
820 "id": "C3494186",
821 "name": "Autosomal Hemophilia A",
822 "type": "Disease",
823 "source": "UMLS"
824 },
825 {
826 "id": "C0042974",
827 "name": "von Willebrand Disease",
828 "type": "Disease",
829 "source": "UMLS"
830 },
831 {
832 "id": "C0015523",
833 "name": "Hereditary Factor XI Deficiency",
834 "type": "Disease",
835 "source": "UMLS"
836 },
837 {
838 "id": "C4016497",
839 "name": "HEMOPHILIA B BRANDENBURG",
840 "type": "Disease",
841 "source": "UMLS"
842 },
843 {
844 "id": "C0272325",
845 "name": "Factor 8 deficiency, acquired",
846 "type": "Disease",
847 "source": "UMLS"
848 },
849 {
850 "id": "C1844137",
851 "name": "Hemophilia A with Vascular Abnormality",
852 "type": "Disease",
853 "source": "UMLS"
854 },
855 {
856 "id": "C3494187",
857 "name": "Factor VIII Deficiency",
858 "type": "Disease",
859 "source": "UMLS"
860 },
861 {
862 "id": "C0272322",
863 "name": "Severe hereditary factor VIII deficiency disease",
864 "type": "Disease",
865 "source": "UMLS"
866 },
867 {
868 "id": "C0272324",
869 "name": "Mild hereditary factor VIII deficiency disease",
870 "type": "Disease",
871 "source": "UMLS"
872 },
873 {
874 "id": "C1307126",
875 "name": "factor VIII, human",
876 "type": "Disease",
877 "source": "UMLS"
878 },
879 {
880 "id": "C0026850",
881 "name": "Muscular Dystrophy",
882 "type": "Disease",
883 "source": "UMLS"
884 },
885 {
886 "id": "C0013264",
887 "name": "Muscular Dystrophy, Duchenne",
888 "type": "Disease",
889 "source": "UMLS"
890 },
891 {
892 "id": "C0238288",
893 "name": "Muscular Dystrophy, Facioscapulohumeral",
894 "type": "Disease",
895 "source": "UMLS"
896 },
897 {
898 "id": "C0917713",
899 "name": "Becker Muscular Dystrophy",
900 "type": "Disease",
901 "source": "UMLS"
902 },
903 {
904 "id": "C0270952",
905 "name": "Muscular Dystrophy, Oculopharyngeal",
906 "type": "Disease",
907 "source": "UMLS"
908 },
909 {
910 "id": "C1450052",
911 "name": "Tibial Muscular Dystrophy",
912 "type": "Disease",
913 "source": "UMLS"
914 },
915 {
916 "id": "C0410192",
917 "name": "Muscular Dystrophy, Scapulohumeral",
918 "type": "Disease",
919 "source": "UMLS"
920 },
921 {
922 "id": "C0699743",
923 "name": "Congenital muscular dystrophy (disorder)",
924 "type": "Disease",
925 "source": "UMLS"
926 },
927 {
928 "id": "C0410174",
929 "name": "Fukuyama Type Congenital Muscular Dystrophy",
930 "type": "Disease",
931 "source": "UMLS"
932 },
933 {
934 "id": "C0026851",
935 "name": "Muscular Dystrophy, Animal",
936 "type": "Disease",
937 "source": "UMLS"
938 },
939 {
940 "id": "C4016477",
941 "name": "INTERMEDIATE MUSCULAR DYSTROPHY",
942 "type": "Disease",
943 "source": "UMLS"
944 },
945 {
946 "id": "C1869123",
947 "name": "Limb-girdle muscular dystrophy type 2A",
948 "type": "Disease",
949 "source": "UMLS"
950 },
951 {
952 "id": "C0410179",
953 "name": "Ullrich congenital muscular dystrophy 1",
954 "type": "Disease",
955 "source": "UMLS"
956 },
957 {
958 "id": "C0410189",
959 "name": "Muscular Dystrophy, Emery-Dreifuss",
960 "type": "Disease",
961 "source": "UMLS"
962 },
963 {
964 "id": "C1858118",
965 "name": "Muscular Dystrophy, Congenital, 1B",
966 "type": "Disease",
967 "source": "UMLS"
968 },
969 {
970 "id": "C1838244",
971 "name": "TIBIAL MUSCULAR DYSTROPHY, TARDIVE",
972 "type": "Disease",
973 "source": "UMLS"
974 },
975 {
976 "id": "C2750076",
977 "name": "Miyoshi Muscular Dystrophy 3",
978 "type": "Disease",
979 "source": "UMLS"
980 },
981 {
982 "id": "C4551973",
983 "name": "Miyoshi Muscular Dystrophy 1",
984 "type": "Disease",
985 "source": "UMLS"
986 },
987 {
988 "id": "C1442927",
989 "name": "Muscular Dystrophy, Cardiac Type",
990 "type": "Disease",
991 "source": "UMLS"
992 },
993 {
994 "id": "C1834673",
995 "name": "Facioscapulohumeral muscular dystrophy 1a",
996 "type": "Disease",
997 "source": "UMLS"
998 },
999 {
1000 "id": "C2750077",
1001 "name": "Miyoshi Muscular Dystrophy 2",
1002 "type": "Disease",
1003 "source": "UMLS"
1004 },
1005 {
1006 "id": "C1834671",
1007 "name": "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B",
1008 "type": "Disease",
1009 "source": "UMLS"
1010 },
1011 {
1012 "id": "C1847759",
1013 "name": "MUSCULAR DYSTROPHY, CONGENITAL, 1C",
1014 "type": "Disease",
1015 "source": "UMLS"
1016 },
1017 {
1018 "id": "C5399970",
1019 "name": "FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1",
1020 "type": "Disease",
1021 "source": "UMLS"
1022 },
1023 {
1024 "id": "C1834688",
1025 "name": "Muscular Dystrophy, Barnes Type",
1026 "type": "Disease",
1027 "source": "UMLS"
1028 },
1029 {
1030 "id": "C0002736",
1031 "name": "Amyotrophic Lateral Sclerosis",
1032 "type": "Disease",
1033 "source": "UMLS"
1034 },
1035 {
1036 "id": "C1862939",
1037 "name": "AMYOTROPHIC LATERAL SCLEROSIS 1",
1038 "type": "Disease",
1039 "source": "UMLS"
1040 },
1041 {
1042 "id": "C2677565",
1043 "name": "Amyotrophic Lateral Sclerosis 10",
1044 "type": "Disease",
1045 "source": "UMLS"
1046 },
1047 {
1048 "id": "C1837728",
1049 "name": "Amyotrophic Lateral Sclerosis 8",
1050 "type": "Disease",
1051 "source": "UMLS"
1052 },
1053 {
1054 "id": "C1865864",
1055 "name": "AMYOTROPHIC LATERAL SCLEROSIS 5",
1056 "type": "Disease",
1057 "source": "UMLS"
1058 },
1059 {
1060 "id": "C1847735",
1061 "name": "Amyotrophic Lateral Sclerosis 3",
1062 "type": "Disease",
1063 "source": "UMLS"
1064 },
1065 {
1066 "id": "C1842674",
1067 "name": "Amyotrophic Lateral Sclerosis 7",
1068 "type": "Disease",
1069 "source": "UMLS"
1070 },
1071 {
1072 "id": "C2678468",
1073 "name": "Amyotrophic Lateral Sclerosis 9",
1074 "type": "Disease",
1075 "source": "UMLS"
1076 },
1077 {
1078 "id": "C2675491",
1079 "name": "AMYOTROPHIC LATERAL SCLEROSIS 11",
1080 "type": "Disease",
1081 "source": "UMLS"
1082 },
1083 {
1084 "id": "C3715155",
1085 "name": "AMYOTROPHIC LATERAL SCLEROSIS 19",
1086 "type": "Disease",
1087 "source": "UMLS"
1088 },
1089 {
1090 "id": "C3715156",
1091 "name": "AMYOTROPHIC LATERAL SCLEROSIS 20",
1092 "type": "Disease",
1093 "source": "UMLS"
1094 },
1095 {
1096 "id": "C3553719",
1097 "name": "AMYOTROPHIC LATERAL SCLEROSIS 18",
1098 "type": "Disease",
1099 "source": "UMLS"
1100 },
1101 {
1102 "id": "C4693381",
1103 "name": "Amyotrophic Lateral Sclerosis 23",
1104 "type": "Disease",
1105 "source": "UMLS"
1106 },
1107 {
1108 "id": "C3150692",
1109 "name": "AMYOTROPHIC LATERAL SCLEROSIS 12",
1110 "type": "Disease",
1111 "source": "UMLS"
1112 },
1113 {
1114 "id": "C3807521",
1115 "name": "AMYOTROPHIC LATERAL SCLEROSIS 21",
1116 "type": "Disease",
1117 "source": "UMLS"
1118 },
1119 {
1120 "id": "C4551993",
1121 "name": "Amyotrophic Lateral Sclerosis, Familial",
1122 "type": "Disease",
1123 "source": "UMLS"
1124 },
1125 {
1126 "id": "C1862941",
1127 "name": "Amyotrophic Lateral Sclerosis, Sporadic",
1128 "type": "Disease",
1129 "source": "UMLS"
1130 },
1131 {
1132 "id": "C5830642",
1133 "name": "AMYOTROPHIC LATERAL SCLEROSIS 28",
1134 "type": "Disease",
1135 "source": "UMLS"
1136 },
1137 {
1138 "id": "C2931786",
1139 "name": "Amyotrophic lateral sclerosis, type 6",
1140 "type": "Disease",
1141 "source": "UMLS"
1142 },
1143 {
1144 "id": "C0543859",
1145 "name": "Amyotrophic Lateral Sclerosis, Guam Form",
1146 "type": "Disease",
1147 "source": "UMLS"
1148 },
1149 {
1150 "id": "C1865409",
1151 "name": "Amyotrophic Lateral Sclerosis 4, Juvenile",
1152 "type": "Disease",
1153 "source": "UMLS"
1154 },
1155 {
1156 "id": "C1859807",
1157 "name": "Amyotrophic Lateral Sclerosis 2, Juvenile",
1158 "type": "Disease",
1159 "source": "UMLS"
1160 },
1161 {
1162 "id": "C0393554",
1163 "name": "Amyotrophic Lateral Sclerosis With Dementia",
1164 "type": "Disease",
1165 "source": "UMLS"
1166 },
1167 {
1168 "id": "C3280587",
1169 "name": "AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE",
1170 "type": "Disease",
1171 "source": "UMLS"
1172 },
1173 {
1174 "id": "C5830359",
1175 "name": "AMYOTROPHIC LATERAL SCLEROSIS 27, JUVENILE",
1176 "type": "Disease",
1177 "source": "UMLS"
1178 },
1179 {
1180 "id": "C0026896",
1181 "name": "Myasthenia Gravis",
1182 "type": "Disease",
1183 "source": "UMLS"
1184 },
1185 {
1186 "id": "C0158982",
1187 "name": "Neonatal Myasthenia Gravis",
1188 "type": "Disease",
1189 "source": "UMLS"
1190 },
1191 {
1192 "id": "C0751340",
1193 "name": "Myasthenia Gravis, Ocular",
1194 "type": "Disease",
1195 "source": "UMLS"
1196 },
1197 {
1198 "id": "C0751339",
1199 "name": "Myasthenia Gravis, Generalized",
1200 "type": "Disease",