MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Carbohydrate Metabolism, Inborn Errors

(UMLS:C0007001)

Definition:: Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero.
UMLS ID:: C0007001
MeSH ID:: D002239

Classification 1:

Name:

Congenital, Hereditary, and Neonatal Diseases and Abnormalities
MeSH Tree Number(s):: C16.320.565.202

Classification 2:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.648.202

Synonym(s)

Carbohydrate Metabolism, Inborn Errors

inborn carbohydrate metabolism disorder

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Dichlorodiphenyl Dichloroethylene		28867213	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Amino Acid Metabolism, Inborn Errors	46.7%
2	Metal Metabolism, Inborn Errors	46.7%
3	Progeria	46.7%
4	Lysosomal Storage Diseases	46.7%
5	Peroxisomal Disorders	46.7%
6	Smith-Lemli-Opitz Syndrome	39.6%
7	Urea Cycle Disorders, Inborn	37.7%
8	Tyrosinemias	37.7%
9	Brain Diseases, Metabolic, Inborn	37.6%
10	Alkaptonuria	34.4%
11	Hypophosphatasia	34.4%
12	Propionic acidemia	34.4%
13	Dihydropyrimidine Dehydrogenase Deficiency	34.4%
14	Cystinosis	34.4%
15	Hyperphosphaturia	33.5%
16	Hypolipoproteinemias	33.3%
17	Cytochrome-c Oxidase Deficiency	33.3%
18	Hyperlipidemia, Familial Combined	32.2%
19	Carbamoyl-Phosphate Synthase I Deficiency Disease	32.1%
20	Hyperlipoproteinemia Type III	31.7%
21	Gaucher Disease	31.5%
22	Homocystinuria	31.2%
23	Pseudohypoparathyroidism	31.1%
24	Hyperhomocysteinemia	30.6%
25	Menkes Kinky Hair Syndrome	30%
26	Hyperlipoproteinemia Type IV	29.9%
27	Hyperlipoproteinemia Type V	29.9%
28	Tay-Sachs Disease	28.6%
29	Fabry Disease	27.6%
30	Adrenoleukodystrophy	27.5%
31	Hypoalphalipoproteinemias	27.5%
32	Niemann-Pick Disease, Type C	27.1%
33	Hepatolenticular Degeneration	26.5%
34	Zellweger Syndrome	26.5%
35	Refsum Disease	26.2%
36	Neuronal Ceroid-Lipofuscinoses	26.2%
37	Werner Syndrome	25.4%
38	Amyloid Neuropathies, Familial	25%
39	Glycogen storage disease type II	24.8%
40	Albinism	24.4%
41	Renal tubular acidosis	23.7%
42	Familial Periodic Paralysis	23.3%
43	Familial Hypophosphatemic Rickets	23.3%
44	Renal Aminoacidurias	22.8%
45	Fanconi Syndrome	22.8%
46	Pseudohypoaldosteronism	22.8%
47	Liddle Syndrome	22.8%
48	Leigh Disease	22.7%
49	Ichthyosis, X-Linked	21.8%
50	Antley-Bixler Syndrome Phenotype	21%
51	Galactosemias	20.7%
52	Wasting Syndrome	20.7%
53	Acid-Base Imbalance	20.5%
54	Calcium Metabolism Disorders	20.5%
55	Iron Metabolism Disorders	20.5%
56	Phosphorus Metabolism Disorders	20.5%
57	Water-Electrolyte Imbalance	20.5%
58	Lipid Metabolism Disorders	20.5%
59	Mitochondrial Diseases	20.5%
60	Glucose Metabolism Disorders	20.5%
61	Gout	20%
62	Hypercalcemia	20%
63	Hypocalcemia	20%
64	Milk-Alkali Syndrome	20%
65	Hypokalemic periodic paralysis	19%
66	Cystinuria	18.8%
67	Sjogren-Larsson Syndrome	18.7%
68	Glycosuria, Renal	18.3%
69	Canavan Disease	17.7%
70	Alexander Disease	17.7%
71	MELAS Syndrome	17.2%
72	Mucopolysaccharidosis II	17.1%
73	Cockayne Syndrome	16.6%
74	Arthritis, Gouty	16.3%
75	Mucopolysaccharidosis III	16.1%
76	Neoplastic Syndromes, Hereditary	16.1%
77	Lipodystrophy	16%
78	Osteopenia	15.5%
79	Brain Diseases, Metabolic	15.3%
80	Multiple Epiphyseal Dysplasia	15.3%
81	Osteochondrodysplasias	15.3%
82	Pelger-Huet Anomaly	15.3%
83	Myasthenic Syndromes, Congenital	15.3%
84	CHARGE Syndrome	14.9%
85	Rickets	14.4%
86	Cystic Fibrosis	14%
87	Aicardi's syndrome	13.9%
88	Fragile X Syndrome	13.9%
89	Porphyrias, Hepatic	13.5%
90	Congenital Hyperinsulinism	13.5%
91	Acidosis	13.3%
92	Alkalosis	13.3%
93	Amyloidosis	13.3%
94	Beckwith-Wiedemann Syndrome	13.3%
95	Bloom Syndrome	13.3%
96	Calcinosis	13.3%
97	Hyperglycemia	13.3%
98	Hyperinsulinism	13.3%
99	Hyperkalemia	13.3%
100	Hypernatremia	13.3%
101	Hypoglycemia	13.3%
102	Hypokalemia	13.3%
103	Hyponatremia	13.3%
104	Familial Mediterranean Fever	13.3%
105	Xanthomatosis	13.3%
106	Hypophosphatemia	13.3%
107	Metabolic acidosis	13.3%
108	Dyslipidemias	13.3%
109	Iron Overload	13.3%
110	Xanthoma	13.3%
111	Wolf-Hirschhorn Syndrome	13.3%
112	Anemia, Sickle Cell	13.2%
113	Thalassemia	13.2%
114	Muscular Dystrophy, Duchenne	13.2%
115	Fanconi Anemia	13.1%
116	Dwarfism	12.7%
117	Nail-Patella Syndrome	12.5%
118	Muscular Dystrophy	12.1%
119	Osteogenesis Imperfecta	12.1%
120	Deformity	11.9%
121	Nutrition Disorders	11.9%
122	Rett Syndrome	11.7%
123	Smith-Magenis syndrome	11.2%
124	Ataxia Telangiectasia	11.2%
125	Cri-du-Chat Syndrome	11%
126	Down Syndrome	11%
127	Trisomy 21	11%
128	Optic Atrophy, Hereditary, Leber	10.9%
129	Osteomalacia	10.9%
130	Prader-Willi Syndrome	10.8%
131	Diabetic Ketoacidosis	10.8%
132	Alstrom Syndrome	10.7%
133	Diabetes Mellitus	10.5%
134	Nesidioblastosis	10.4%
135	Autoimmune Lymphoproliferative Syndrome	10.2%
136	Dehydration	10.2%
137	Lipomatosis	10.2%
138	Water Intoxication	10.2%
139	Achlorhydria	10%
140	Osteoporosis	10%
141	Bone Demineralization, Pathologic	10%
142	Post-Traumatic Osteoporosis	10%
143	Angioedemas, Hereditary	9.9%
144	Celiac Disease	9.9%
145	Sprue, Tropical	9.9%
146	Steatorrhea	9.9%
147	Sprue	9.9%
148	Wiskott-Aldrich Syndrome	9.9%
149	Acidosis, Lactic	9.9%
150	Calciphylaxis	9.9%
151	Hemosiderosis	9.9%
152	Ketosis	9.9%
153	Ketonuria	9.9%
154	Ketoacidosis	9.9%
155	Ketonemia	9.9%
156	Vascular calcification	9.9%
157	Mitochondrial Encephalomyopathies	9.9%
158	Variegate Porphyria	9.8%
159	Acute intermittent porphyria	9.8%
160	Porphyria Cutanea Tarda	9.8%
161	Friedreich Ataxia	9.8%
162	Sickle Cell Trait	9.7%
163	Holoprosencephaly	9.6%
164	Ectodermal Dysplasia	9.5%
165	Aplasia Cutis Congenita	9.5%
166	Xeroderma Pigmentosum	9.4%
167	Marfan Syndrome	9.4%
168	Kartagener Syndrome	9.3%
169	Fetal Diseases	8.9%
170	Primary Ciliary Dyskinesia	8.9%
171	Myotonic Dystrophy	8.8%
172	Polycystic Kidney Diseases	8.8%
173	Williams Syndrome	8.8%
174	Kallmann Syndrome	8.4%
175	Rubinstein-Taybi Syndrome	8.4%
176	Hypercholesterolemia	8.2%
177	Hyperlipoproteinemias	8.2%
178	Hypertriglyceridemia	8.2%
179	Tuberous Sclerosis	8.2%
180	Cutis Laxa	8.1%
181	Mitochondrial Myopathies	8.1%
182	Retinitis Pigmentosa	8.1%
183	Myelinolysis, Central Pontine	8.1%
184	Pigmentary retinopathy	8.1%
185	Porokeratosis	8%
186	Keratoderma, Palmoplantar	8%
187	Glycosuria	7.9%
188	Chronic granulomatous disease	7.9%
189	Reye Syndrome	7.9%
190	Hepatic Encephalopathy	7.9%
191	Welander Distal Myopathy	7.9%
192	Retinal Dysplasia	7.8%
193	Aniridia	7.8%
194	Epidermolysis Bullosa	7.6%
195	HIV Wasting Syndrome	7.5%
196	Acute Chest Syndrome	7.5%
197	Acidosis, Respiratory	7.4%
198	Adiposis Dolorosa	7.4%
199	Alkalosis, Respiratory	7.4%
200	Insulin Resistance	7.4%
201	Osteoporosis, Postmenopausal	7.4%
202	HIV-Associated Lipodystrophy Syndrome	7.3%
203	Renal Osteodystrophy	7.3%
204	Renal rickets	7.3%
205	Abdominal Cramps	6.8%
206	Abnormalities, Drug-Induced	6.8%
207	Amniotic Band Syndrome	6.8%
208	Asphyxia Neonatorum	6.8%
209	Child Nutrition Disorders	6.8%
210	Duane Retraction Syndrome	6.8%
211	Hypervitaminosis A	6.8%
212	Infant Nutrition Disorders	6.8%
213	Infant, Premature, Diseases	6.8%
214	Situs Inversus	6.8%
215	Malnutrition	6.8%
216	Infantile Colic	6.8%
217	Kernicterus	6.7%
218	Peutz-Jeghers Syndrome	6.6%
219	Wernicke Encephalopathy	6.6%
220	Myotonia Congenita	6.6%
221	Thrombasthenia	6.6%
222	Antithrombin III Deficiency	6.6%
223	Necrobiosis Lipoidica Diabeticorum	6.6%
224	Protein C Deficiency	6.6%
225	Afibrinogenemia	6.6%
226	Dystonia Musculorum Deformans	6.6%
227	Factor VII Deficiency	6.6%
228	Factor X Deficiency	6.6%
229	Factor XII Deficiency	6.6%
230	Hemophilia A	6.6%
231	Activated Protein C Resistance	6.6%
232	Factor II deficiency	6.6%
233	Factor VIII Deficiency	6.6%
234	Factor V deficiency	6.6%
235	Factor XI Deficiency	6.6%
236	Hypoprothrombinemias	6.6%
237	Lactose Intolerance	6.6%
238	Lafora Disease	6.5%
239	Unverricht-Lundborg Syndrome	6.5%
240	Anemia, Diamond-Blackfan	6.5%
241	Polycystic Kidney, Autosomal Dominant	6.5%
242	Classical Lissencephalies and Subcortical Band Heterotopias	6.3%
243	Gestational Diabetes	6.1%
244	Latent Autoimmune Diabetes in Adults	6.1%
245	Diabetes Mellitus, Experimental	6%
246	Pseudoxanthoma Elasticum	5.9%
247	Nephrocalcinosis	5.9%
248	Tetany	5.9%
249	Meconium Aspiration Syndrome	5.9%
250	Multiple Endocrine Neoplasia	5.9%
251	Papillon-Lefevre Disease	5.9%
252	Hyperkeratosis, Epidermolytic	5.9%
253	Cerebral Amyloid Angiopathy	5.8%
254	Congenital Hypothyroidism	5.7%
255	Dermatitis, Atopic	5.7%
256	Xeroderma	5.6%
257	Mobius Syndrome	5.6%
258	Charcot-Marie-Tooth Disease	5.6%
259	Eye Abnormalities	5.4%
260	Cardiovascular Abnormalities	5.4%
261	Kearns-Sayre syndrome	5.3%
262	Skin Abnormalities	5.2%
263	Lymphatic Abnormalities	5.2%
264	Congenital Microtia	5.2%
265	Anemia, Neonatal	5.1%
266	Persistent Fetal Circulation Syndrome	5.1%
267	Congenital diaphragmatic hernia	5%
268	Umbilical hernia	5%
269	Behcet Syndrome	5%
270	Primary amyloidosis	5%
271	Basal Cell Nevus Syndrome	4.8%
272	Anencephaly	4.6%
273	Klinefelter Syndrome	4.5%
274	Deficiency Diseases	4.4%
275	Prune Belly Syndrome	4.4%
276	Starvation	4.4%
277	Twins, Conjoined	4.4%
278	Refeeding Syndrome	4.4%
279	Waardenburg Syndrome	4.4%
280	Huntington Disease	4.4%
281	Urogenital Abnormalities	4.3%
282	Amyotrophic Lateral Sclerosis	4.3%
283	Multiple Endocrine Neoplasia Type 1	4.2%
284	Hydrops Fetalis	4.2%
285	Neonatal Abstinence Syndrome	4.2%
286	Fetal Growth Retardation	4.1%
287	Frontotemporal dementia	4.1%
288	Fetal Hypoxia	4%
289	Congenital nystagmus	4%
290	Fetal Alcohol Spectrum Disorders	4%
291	Toxoplasmosis, Congenital	4%
292	Syphilis, Congenital	4%
293	Nephroblastoma	3.9%
294	Maxillofacial Abnormalities	3.9%
295	Dural Arteriovenous Fistula	3.9%
296	Turner Syndrome	3.9%
297	Dextrocardia	3.9%
298	CREST Syndrome	3.7%
299	Adenomatous Polyposis Coli	3.5%
300	Anophthalmos	3.4%
301	Anus, Imperforate	3.4%
302	Hydranencephaly	3.4%
303	Microphthalmos	3.4%
304	Neural Tube Defects	3.4%
305	Paralysis, Obstetric	3.4%
306	Retinopathy of Prematurity	3.4%
307	Tethered Cord Syndrome	3.4%
308	Iniencephaly	3.4%
309	Craniorachischisis	3.4%
310	Limb Deformities, Congenital	3.4%
311	Exencephaly	3.4%
312	Septo-Optic Dysplasia	3.4%
313	Craniofacial Abnormalities	3.4%
314	Cortical Dysplasia	3.4%
315	Malformations of Cortical Development	3.4%
316	Anorectal Malformations	3.4%
317	Chorioamnionitis	3.4%
318	Bronchopulmonary Dysplasia	3.3%
319	Kwashiorkor	3.3%
320	Magnesium Deficiency	3.3%
321	Potassium Deficiency	3.3%
322	Protein Deficiency	3.3%
323	Avitaminosis	3.3%
324	Microcephaly	3%
325	Macrocephaly	3%
326	Scimitar Syndrome	3%
327	Abnormalities, Radiation-Induced	2.9%
328	Craniosynostosis	2.8%
329	Syndactyly	2.8%
330	Brachycephaly	2.8%
331	Blepharophimosis	2.7%
332	Laryngostenosis	2.7%
333	Mouth Abnormalities	2.7%
334	Respiratory Distress Syndrome, Newborn	2.7%
335	Ascorbic Acid Deficiency	2.7%
336	Vitamin A Deficiency	2.7%
337	Vitamin D Deficiency	2.7%
338	Vitamin E Deficiency	2.7%
339	Marasmus	2.7%
340	Esophageal Atresia	2.7%
341	Intestinal Atresia	2.7%
342	Horseshoe Kidney	2.7%
343	Pectus excavatum	2.7%
344	Porencephaly	2.7%
345	Klippel-Feil Syndrome	2.7%
346	Gastroschisis	2.7%
347	Synostosis	2.7%
348	Acrocephalosyndactylia	2.7%
349	Acrodermatitis	2.7%
350	Lymphangiectasis, Intestinal	2.7%
351	Gianotti-Crosti Syndrome	2.7%
352	Denys-Drash Syndrome	2.6%
353	Noonan Syndrome	2.5%
354	Amelia	2.5%
355	Arachnodactyly	2.5%
356	Ectopia Cordis	2.5%
357	Ectromelia	2.5%
358	Hemimelia	2.5%
359	Meningomyelocele	2.5%
360	Phocomelia	2.5%
361	Sirenomelia	2.5%
362	Spina Bifida	2.5%
363	Polydactyly	2.5%
364	Brachydactyly	2.5%
365	Plagiocephaly	2.5%
366	Lower Extremity Deformities, Congenital	2.5%
367	Upper Extremity Deformities, Congenital	2.5%
368	Single umbilical artery	2.5%
369	Ophthalmia Neonatorum	2.5%
370	Folic Acid Deficiency	2.5%
371	Pellagra	2.5%
372	Thiamine Deficiency	2.5%
373	Vitamin B 12 Deficiency	2.5%
374	Vitamin B 6 Deficiency	2.5%
375	Pyridoxine Deficiency	2.5%
376	Beriberi	2.3%
377	Poland Syndrome	2.3%
378	Cleft Palate	2.3%
379	Arthrogryposis	2.3%
380	Choanal Atresia	2.3%
381	Tracheobronchomegaly	2.3%
382	Laryngocele	2.3%
383	Jaw Abnormalities	2.3%
384	Choledochal Cyst	2.3%
385	Hermaphroditism	2.3%
386	Disorders of Sex Development	2.3%
387	Cryptorchidism	2.2%
388	Hypospadias	2.2%
389	Central Nervous System Cysts	2.2%
390	Dandy-Walker Syndrome	2.2%
391	Leukomalacia, Periventricular	2.2%
392	POEMS Syndrome	2.2%
393	Obesity	2.2%
394	Dermal Sinus	2%
395	Spina Bifida Cystica	2%
396	Spina Bifida Occulta	2%
397	Lissencephaly	2%
398	Polymicrogyria	2%
399	Pachygyria	2%
400	Schizencephaly	2%
401	Periventricular Nodular Heterotopia	2%
402	Aortic coarctation	2%
403	Cor Triatriatum	2%
404	Coronary Vessel Anomalies	2%
405	Dental Enamel Hypoplasia	2%
406	Patent ductus arteriosus	2%
407	Ebstein Anomaly	2%
408	Heart Septal Defects	2%
409	Hyaline Membrane Disease	2%
410	Hypodontia	2%
411	Macrostomia	2%
412	Meningocele	2%
413	Microstomia	2%
414	Tetralogy of Fallot	2%
415	Transposition of Great Vessels	2%
416	Hypoplastic Left Heart Syndrome	2%
417	May-Thurner Syndrome	2%
418	Encephalocele	2%
419	Craniofacial Dysostosis	2%
420	Wolff-Parkinson-White Syndrome	2%
421	Laryngomalacia	2%
422	Pectus carinatum	1.9%
423	Obesity, Abdominal	1.9%
424	Micrognathism	1.9%
425	Pierre Robin Syndrome	1.9%
426	Bladder Exstrophy	1.9%
427	Epispadias	1.9%
428	Multicystic Dysplastic Kidney	1.9%
429	Retrognathia	1.7%
430	Anemia, Pernicious	1.7%
431	Long QT Syndrome	1.7%
432	Platybasia	1.7%
433	Tricuspid Atresia	1.7%
434	Arrhythmogenic Right Ventricular Dysplasia	1.7%
435	Vitamin K Deficiency	1.7%
436	Gonadal Dysgenesis	1.6%
437	Bronchomalacia	1.6%
438	Adrenogenital Syndrome	1.6%
439	Tracheomalacia	1.6%
440	Ovotesticular Disorders of Sex Development	1.6%
441	Aortopulmonary Septal Defect	1.6%
442	Double Outlet Right Ventricle	1.6%
443	Endocardial Cushion Defects	1.6%
444	Myocardial bridging	1.6%
445	Aorticopulmonary Septal Defect	1.6%
446	Hyperandrogenism	1.6%
447	Pediatric Obesity	1.6%
448	Prognathism	1.6%
449	Scurvy	1.5%
450	Truncus Arteriosus, Persistent	1.5%
451	Goldenhar Syndrome	1.5%
452	Mandibulofacial Dysostosis	1.4%
453	Romano-Ward Syndrome	1.4%
454	Talipes	1.2%
455	Congenital clubfoot	1.1%
456	Vertical Talus	1.1%
457	Arteriovenous fistula	1%
458	Subacute Combined Degeneration	1%

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