MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Glycogen Storage Disease Type V

(UMLS:C0017924)

Definition:: Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
UMLS ID:: C0017924
MeSH ID:: D006012

Classification 1:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.320.565.202.449.560

Classification 2:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.648.202.449.560

Synonym(s)

Glycogen Storage Disease Type V

GLYCOGEN STORAGE DISEASE V

GLYCOGENOSIS, TYPE V

GSD V

GSD type V

Glycogen storage disease type 5

Glycogen storage disease type V

Glycogen storage disease, type V

Glycogenosis, type 5

10.

MCARDLE DISEASE

11.

MUSCLE PHOSPHORYLASE DEFICIENCY

12.

MYOPHOSPHORYLASE DEFICIENCY

13.

MYOPHOSPHORYLASE DEFICIENCY GLYCOGENOSIS

14.

McArdle

15.

McArdle disease

16.

McArdle's disease

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Simvastatin	FAERS: 11		US FAERS
2	Rosuvastatin Calcium	FAERS: 3		US FAERS
3	Adrenocorticotropic Hormone		4313853	CTD
4	Danazol			OFFSIDES
5	Raloxifene Hydrochloride			OFFSIDES
6	tizanidine			OFFSIDES

Similar ADE(s)

	Name	Semantic Similarity
1	Glycogen Storage Disease Type I	49.2%
2	Glycogen storage disease type II	29.5%
3	Amino Acid Metabolism, Inborn Errors	28.5%
4	Metal Metabolism, Inborn Errors	28.5%
5	Progeria	28.5%
6	Lysosomal Storage Diseases	28.5%
7	Peroxisomal Disorders	28.5%
8	Galactosemias	28.3%
9	Lactose Intolerance	28.2%
10	Brain Diseases, Metabolic, Inborn	23.1%
11	Leigh Disease	22.5%
12	Cytochrome-c Oxidase Deficiency	20.3%
13	Mucopolysaccharidosis III	20%
14	Smith-Lemli-Opitz Syndrome	19.8%
15	Urea Cycle Disorders, Inborn	18.6%
16	Tyrosinemias	18.6%
17	Werner Syndrome	17.4%
18	Mucopolysaccharidosis II	16.9%
19	Alkaptonuria	16.8%
20	Hypophosphatasia	16.8%
21	Propionic acidemia	16.8%
22	Dihydropyrimidine Dehydrogenase Deficiency	16.8%
23	Cystinosis	16.8%
24	Pseudohypoparathyroidism	16.7%
25	Hyperphosphaturia	16.6%
26	Hypolipoproteinemias	16.3%
27	Hyperhomocysteinemia	15.7%
28	Hyperlipidemia, Familial Combined	15.3%
29	Wasting Syndrome	15.1%
30	Menkes Kinky Hair Syndrome	14.9%
31	Acid-Base Imbalance	14.8%
32	Calcium Metabolism Disorders	14.8%
33	Iron Metabolism Disorders	14.8%
34	Phosphorus Metabolism Disorders	14.8%
35	Water-Electrolyte Imbalance	14.8%
36	Lipid Metabolism Disorders	14.8%
37	Mitochondrial Diseases	14.8%
38	Glucose Metabolism Disorders	14.8%
39	Hyperlipoproteinemia Type III	14.8%
40	Homocystinuria	14.2%
41	Carbamoyl-Phosphate Synthase I Deficiency Disease	13.6%
42	Hepatolenticular Degeneration	13.6%
43	Hyperlipoproteinemia Type IV	13.5%
44	Hyperlipoproteinemia Type V	13.5%
45	Zellweger Syndrome	13.3%
46	Albinism	13.1%
47	Refsum Disease	13%
48	Adrenoleukodystrophy	12.9%
49	Amyloid Neuropathies, Familial	12.4%
50	Hypercalcemia	12.2%
51	Hypocalcemia	12.2%
52	Milk-Alkali Syndrome	12.2%
53	Neuronal Ceroid-Lipofuscinoses	12%
54	Ichthyosis, X-Linked	11.8%
55	Neoplastic Syndromes, Hereditary	11.7%
56	Renal tubular acidosis	11.7%
57	Familial Periodic Paralysis	11.5%
58	Osteopenia	11.3%
59	Renal Aminoacidurias	11.2%
60	Fanconi Syndrome	11.2%
61	Pseudohypoaldosteronism	11.2%
62	Liddle Syndrome	11.2%
63	Brain Diseases, Metabolic	11.2%
64	Multiple Epiphyseal Dysplasia	11.2%
65	Osteochondrodysplasias	11.2%
66	Pelger-Huet Anomaly	11.2%
67	Myasthenic Syndromes, Congenital	11.2%
68	Hypoalphalipoproteinemias	10.8%
69	CHARGE Syndrome	10.6%
70	Gaucher Disease	10.5%
71	Antley-Bixler Syndrome Phenotype	10.3%
72	Cystic Fibrosis	10.3%
73	Cockayne Syndrome	10.2%
74	Fabry Disease	10%
75	Gout	9.9%
76	Lipodystrophy	9.8%
77	Deformity	9.8%
78	Nutrition Disorders	9.8%
79	Dwarfism	9.3%
80	Familial Hypophosphatemic Rickets	9.2%
81	Glycosuria, Renal	9.1%
82	Nail-Patella Syndrome	8.9%
83	Muscular Dystrophy	8.9%
84	Osteogenesis Imperfecta	8.9%
85	Sjogren-Larsson Syndrome	8.8%
86	Aicardi's syndrome	8.7%
87	Rickets	8.5%
88	Porphyrias, Hepatic	8.3%
89	MELAS Syndrome	8.3%
90	Beckwith-Wiedemann Syndrome	8.2%
91	Wolf-Hirschhorn Syndrome	8.2%
92	Anemia, Sickle Cell	8.1%
93	Bloom Syndrome	8.1%
94	Thalassemia	8.1%
95	Muscular Dystrophy, Duchenne	8.1%
96	Acidosis	8.1%
97	Alkalosis	8.1%
98	Amyloidosis	8.1%
99	Calcinosis	8.1%
100	Fanconi Anemia	8.1%
101	Hyperglycemia	8.1%
102	Hyperinsulinism	8.1%
103	Hyperkalemia	8.1%
104	Hypernatremia	8.1%
105	Hypoglycemia	8.1%
106	Hypokalemia	8.1%
107	Hyponatremia	8.1%
108	Familial Mediterranean Fever	8.1%
109	Xanthomatosis	8.1%
110	Hypophosphatemia	8.1%
111	Metabolic acidosis	8.1%
112	Dyslipidemias	8.1%
113	Iron Overload	8.1%
114	Xanthoma	8.1%
115	Niemann-Pick Disease, Type C	8%
116	Canavan Disease	7.9%
117	Alexander Disease	7.9%
118	Ataxia Telangiectasia	7.8%
119	Tay-Sachs Disease	7.8%
120	Autoimmune Lymphoproliferative Syndrome	7.5%
121	Hypokalemic periodic paralysis	7.5%
122	Congenital Hyperinsulinism	7.5%
123	Cystinuria	7.4%
124	Fetal Diseases	7.4%
125	Angioedemas, Hereditary	7.3%
126	Smith-Magenis syndrome	6.9%
127	Fragile X Syndrome	6.9%
128	Cri-du-Chat Syndrome	6.8%
129	Down Syndrome	6.8%
130	Trisomy 21	6.8%
131	Prader-Willi Syndrome	6.5%
132	Marfan Syndrome	6.5%
133	Arthritis, Gouty	6.4%
134	Diabetes Mellitus	6.4%
135	Dehydration	6.2%
136	Lipomatosis	6.2%
137	Water Intoxication	6.2%
138	Wiskott-Aldrich Syndrome	6.1%
139	Achlorhydria	6.1%
140	Osteoporosis	6.1%
141	Bone Demineralization, Pathologic	6.1%
142	Post-Traumatic Osteoporosis	6.1%
143	Celiac Disease	6%
144	Sprue, Tropical	6%
145	Steatorrhea	6%
146	Sprue	6%
147	Optic Atrophy, Hereditary, Leber	5.9%
148	Kallmann Syndrome	5.9%
149	Ectodermal Dysplasia	5.9%
150	Aplasia Cutis Congenita	5.9%
151	Xeroderma Pigmentosum	5.8%
152	Rett Syndrome	5.8%
153	Alstrom Syndrome	5.7%
154	Kartagener Syndrome	5.7%
155	Holoprosencephaly	5.6%
156	Mitochondrial Encephalomyopathies	5.6%
157	Friedreich Ataxia	5.5%
158	Myotonic Dystrophy	5.4%
159	Polycystic Kidney Diseases	5.4%
160	Williams Syndrome	5.4%
161	Primary Ciliary Dyskinesia	5.2%
162	Osteomalacia	5.1%
163	Rubinstein-Taybi Syndrome	5.1%
164	Cutis Laxa	5%
165	Mitochondrial Myopathies	5%
166	Abdominal Cramps	4.9%
167	Abnormalities, Drug-Induced	4.9%
168	Amniotic Band Syndrome	4.9%
169	Asphyxia Neonatorum	4.9%
170	Child Nutrition Disorders	4.9%
171	Hypervitaminosis A	4.9%
172	Infant Nutrition Disorders	4.9%
173	Infant, Premature, Diseases	4.9%
174	Situs Inversus	4.9%
175	Malnutrition	4.9%
176	Infantile Colic	4.9%
177	Retinitis Pigmentosa	4.9%
178	Myelinolysis, Central Pontine	4.9%
179	Pigmentary retinopathy	4.9%
180	Porokeratosis	4.9%
181	Keratoderma, Palmoplantar	4.9%
182	Tuberous Sclerosis	4.9%
183	Glycosuria	4.9%
184	Chronic granulomatous disease	4.9%
185	Reye Syndrome	4.9%
186	Hepatic Encephalopathy	4.8%
187	Variegate Porphyria	4.8%
188	Acute intermittent porphyria	4.8%
189	Porphyria Cutanea Tarda	4.8%
190	Retinal Dysplasia	4.8%
191	Diabetic Ketoacidosis	4.8%
192	Welander Distal Myopathy	4.8%
193	Sickle Cell Trait	4.8%
194	Acidosis, Lactic	4.8%
195	Calciphylaxis	4.8%
196	Hemosiderosis	4.8%
197	Ketosis	4.8%
198	Ketonuria	4.8%
199	Ketoacidosis	4.8%
200	Ketonemia	4.8%
201	Vascular calcification	4.8%
202	Aniridia	4.8%
203	Epidermolysis Bullosa	4.7%
204	HIV Wasting Syndrome	4.6%
205	Nesidioblastosis	4.6%
206	Meconium Aspiration Syndrome	4.3%
207	Duane Retraction Syndrome	4.2%
208	Kernicterus	4.1%
209	Peutz-Jeghers Syndrome	4.1%
210	Myotonia Congenita	4.1%
211	Thrombasthenia	4.1%
212	Antithrombin III Deficiency	4.1%
213	Necrobiosis Lipoidica Diabeticorum	4.1%
214	Protein C Deficiency	4.1%
215	Afibrinogenemia	4.1%
216	Dystonia Musculorum Deformans	4.1%
217	Factor VII Deficiency	4.1%
218	Factor X Deficiency	4.1%
219	Factor XII Deficiency	4.1%
220	Hemophilia A	4.1%
221	Activated Protein C Resistance	4.1%
222	Factor II deficiency	4.1%
223	Factor VIII Deficiency	4.1%
224	Factor V deficiency	4.1%
225	Factor XI Deficiency	4.1%
226	Hypoprothrombinemias	4.1%
227	Lafora Disease	4%
228	Unverricht-Lundborg Syndrome	4%
229	Anemia, Diamond-Blackfan	4%
230	Eye Abnormalities	3.9%
231	Cardiovascular Abnormalities	3.9%
232	Xeroderma	3.9%
233	Mobius Syndrome	3.9%
234	Skin Abnormalities	3.8%
235	Lymphatic Abnormalities	3.8%
236	Congenital Microtia	3.8%
237	Wernicke Encephalopathy	3.8%
238	Anemia, Neonatal	3.7%
239	Persistent Fetal Circulation Syndrome	3.7%
240	Acute Chest Syndrome	3.7%
241	Congenital diaphragmatic hernia	3.7%
242	Pseudoxanthoma Elasticum	3.7%
243	Umbilical hernia	3.7%
244	Acidosis, Respiratory	3.6%
245	Adiposis Dolorosa	3.6%
246	Alkalosis, Respiratory	3.6%
247	Multiple Endocrine Neoplasia	3.6%
248	HIV-Associated Lipodystrophy Syndrome	3.6%
249	Insulin Resistance	3.6%
250	Osteoporosis, Postmenopausal	3.6%
251	Congenital Hypothyroidism	3.5%
252	Dermatitis, Atopic	3.5%
253	Renal Osteodystrophy	3.4%
254	Renal rickets	3.4%
255	Polycystic Kidney, Autosomal Dominant	3.2%
256	Hypercholesterolemia	3.2%
257	Hyperlipoproteinemias	3.2%
258	Hypertriglyceridemia	3.2%
259	Urogenital Abnormalities	3.1%
260	Behcet Syndrome	3.1%
261	Neonatal Abstinence Syndrome	3.1%
262	Gestational Diabetes	3%
263	Latent Autoimmune Diabetes in Adults	3%
264	Fetal Growth Retardation	3%
265	Basal Cell Nevus Syndrome	3%
266	Diabetes Mellitus, Experimental	3%
267	Fetal Hypoxia	3%
268	Congenital nystagmus	3%
269	Fetal Alcohol Spectrum Disorders	3%
270	Toxoplasmosis, Congenital	2.9%
271	Syphilis, Congenital	2.9%
272	Nephrocalcinosis	2.9%
273	Tetany	2.9%
274	Papillon-Lefevre Disease	2.9%
275	Cerebral Amyloid Angiopathy	2.9%
276	Classical Lissencephalies and Subcortical Band Heterotopias	2.8%
277	Kearns-Sayre syndrome	2.8%
278	Hyperkeratosis, Epidermolytic	2.8%
279	Charcot-Marie-Tooth Disease	2.8%
280	Huntington Disease	2.7%
281	Deficiency Diseases	2.7%
282	Prune Belly Syndrome	2.7%
283	Starvation	2.7%
284	Twins, Conjoined	2.7%
285	Refeeding Syndrome	2.7%
286	Waardenburg Syndrome	2.7%
287	Anencephaly	2.6%
288	Chorioamnionitis	2.5%
289	Primary amyloidosis	2.4%
290	Nephroblastoma	2.4%
291	Adenomatous Polyposis Coli	2.2%
292	Maxillofacial Abnormalities	2.2%
293	Dural Arteriovenous Fistula	2.2%
294	Dextrocardia	2.2%
295	Abnormalities, Radiation-Induced	2.1%
296	Amyotrophic Lateral Sclerosis	2.1%
297	Multiple Endocrine Neoplasia Type 1	2.1%
298	Anophthalmos	2.1%
299	Anus, Imperforate	2.1%
300	Hydranencephaly	2.1%
301	Microphthalmos	2.1%
302	Neural Tube Defects	2.1%
303	Paralysis, Obstetric	2.1%
304	Retinopathy of Prematurity	2.1%
305	Tethered Cord Syndrome	2.1%
306	Iniencephaly	2.1%
307	Craniorachischisis	2.1%
308	Limb Deformities, Congenital	2.1%
309	Exencephaly	2.1%
310	Septo-Optic Dysplasia	2.1%
311	Craniofacial Abnormalities	2.1%
312	Cortical Dysplasia	2.1%
313	Malformations of Cortical Development	2.1%
314	Anorectal Malformations	2.1%
315	Bronchopulmonary Dysplasia	2%
316	Hydrops Fetalis	2%
317	Ophthalmia Neonatorum	1.8%
318	CREST Syndrome	1.8%
319	Klinefelter Syndrome	1.8%
320	Scimitar Syndrome	1.7%
321	Blepharophimosis	1.7%
322	Laryngostenosis	1.7%
323	Mouth Abnormalities	1.7%
324	Respiratory Distress Syndrome, Newborn	1.7%
325	Esophageal Atresia	1.7%
326	Intestinal Atresia	1.7%
327	Horseshoe Kidney	1.7%
328	Pectus excavatum	1.7%
329	Klippel-Feil Syndrome	1.6%
330	Gastroschisis	1.6%
331	Synostosis	1.6%
332	Acrodermatitis	1.6%
333	Lymphangiectasis, Intestinal	1.6%
334	Gianotti-Crosti Syndrome	1.6%
335	Turner Syndrome	1.6%
336	Kwashiorkor	1.6%
337	Magnesium Deficiency	1.6%
338	Potassium Deficiency	1.6%
339	Protein Deficiency	1.6%
340	Frontotemporal dementia	1.6%
341	Avitaminosis	1.6%
342	Arthrogryposis	1.4%
343	Choanal Atresia	1.4%
344	Tracheobronchomegaly	1.4%
345	Laryngocele	1.4%
346	Choledochal Cyst	1.4%
347	Hermaphroditism	1.4%
348	Disorders of Sex Development	1.4%
349	Craniosynostosis	1.4%
350	Syndactyly	1.4%
351	Brachycephaly	1.4%
352	Cryptorchidism	1.4%
353	Hypospadias	1.4%
354	Central Nervous System Cysts	1.4%
355	Dandy-Walker Syndrome	1.4%
356	Leukomalacia, Periventricular	1.4%
357	POEMS Syndrome	1.4%
358	Microcephaly	1.3%
359	Macrocephaly	1.3%
360	Obesity	1.3%
361	Denys-Drash Syndrome	1.3%
362	Noonan Syndrome	1.2%
363	Amelia	1.2%
364	Arachnodactyly	1.2%
365	Ectopia Cordis	1.2%
366	Ectromelia	1.2%
367	Hemimelia	1.2%
368	Meningomyelocele	1.2%
369	Phocomelia	1.2%
370	Sirenomelia	1.2%
371	Spina Bifida	1.2%
372	Polydactyly	1.2%
373	Brachydactyly	1.2%
374	Plagiocephaly	1.2%
375	Lower Extremity Deformities, Congenital	1.2%
376	Upper Extremity Deformities, Congenital	1.2%
377	Single umbilical artery	1.2%
378	Laryngomalacia	1.2%
379	Pectus carinatum	1.2%
380	Bladder Exstrophy	1.2%
381	Epispadias	1.2%
382	Multicystic Dysplastic Kidney	1.2%
383	Porencephaly	1.1%
384	Acrocephalosyndactylia	1.1%
385	Ascorbic Acid Deficiency	1.1%
386	Vitamin A Deficiency	1.1%
387	Vitamin D Deficiency	1.1%
388	Vitamin E Deficiency	1.1%
389	Marasmus	1.1%
390	Jaw Abnormalities	1%
391	Aortic coarctation	1%
392	Cor Triatriatum	1%
393	Coronary Vessel Anomalies	1%
394	Dental Enamel Hypoplasia	1%
395	Patent ductus arteriosus	1%
396	Ebstein Anomaly	1%
397	Heart Septal Defects	1%
398	Hyaline Membrane Disease	1%
399	Hypodontia	1%
400	Macrostomia	1%
401	Meningocele	1%
402	Microstomia	1%
403	Tetralogy of Fallot	1%
404	Transposition of Great Vessels	1%
405	Hypoplastic Left Heart Syndrome	1%
406	May-Thurner Syndrome	1%
407	Encephalocele	1%
408	Craniofacial Dysostosis	1%
409	Wolff-Parkinson-White Syndrome	1%
410	Cleft Palate	1%
411	Obesity, Abdominal	1%
412	Poland Syndrome	0.9%
413	Long QT Syndrome	0.8%
414	Platybasia	0.8%
415	Tricuspid Atresia	0.8%
416	Arrhythmogenic Right Ventricular Dysplasia	0.8%
417	Gonadal Dysgenesis	0.8%
418	Bronchomalacia	0.8%
419	Adrenogenital Syndrome	0.8%
420	Tracheomalacia	0.8%
421	Ovotesticular Disorders of Sex Development	0.8%
422	Dermal Sinus	0.8%
423	Spina Bifida Cystica	0.8%
424	Spina Bifida Occulta	0.8%
425	Lissencephaly	0.8%
426	Polymicrogyria	0.8%
427	Pachygyria	0.8%
428	Schizencephaly	0.8%
429	Periventricular Nodular Heterotopia	0.8%
430	Pediatric Obesity	0.8%
431	Folic Acid Deficiency	0.8%
432	Pellagra	0.8%
433	Thiamine Deficiency	0.8%
434	Vitamin B 12 Deficiency	0.8%
435	Vitamin B 6 Deficiency	0.8%
436	Pyridoxine Deficiency	0.8%
437	Micrognathism	0.7%
438	Pierre Robin Syndrome	0.7%
439	Beriberi	0.7%
440	Vitamin K Deficiency	0.6%
441	Aortopulmonary Septal Defect	0.6%
442	Double Outlet Right Ventricle	0.6%
443	Endocardial Cushion Defects	0.6%
444	Hyperandrogenism	0.6%
445	Myocardial bridging	0.6%
446	Aorticopulmonary Septal Defect	0.6%
447	Retrognathia	0.6%
448	Prognathism	0.6%
449	Mandibulofacial Dysostosis	0.5%
450	Romano-Ward Syndrome	0.5%
451	Anemia, Pernicious	0.5%
452	Scurvy	0.5%
453	Truncus Arteriosus, Persistent	0.5%
454	Goldenhar Syndrome	0.5%
455	Arteriovenous fistula	0.4%
456	Talipes	0.4%
457	Congenital clubfoot	0.3%
458	Vertical Talus	0.3%
459	Subacute Combined Degeneration	0.3%

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