MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Hypophosphatemia

(UMLS:C0085682)

Definition:: A condition of an abnormally low level of PHOSPHATES in the blood.
UMLS ID:: C0085682
MeSH ID:: D017674

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.750.400

Synonym(s)

Hypophosphatemia

Disorder characterized by hypophosphatemia

HYPOPHOSPHATAEMIA

HYPOPHOSPHATEMIA

Hypophosphataemia

Hypophosphataemia, NOS

Hypophosphatemia, NOS

Low blood phosphate level

disorder hypophosphatemia

10.

hypophosphataemia

11.

hypophosphatemia

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Acetaminophen	3120990 7979097 10462288	CTD
2	Acyclovir	8456495 14675048	CTD
3	Azacitidine	6160887	CTD
4	Betamethasone	16830158	CTD
5	Bupivacaine	16830158	CTD
6	Capecitabine	19584382	CTD
7	Clobazam	7624000	CTD
8	Crizotinib	22954507	CTD
9	Demeclocycline	8450917	CTD
10	Doxycycline	3277077	CTD
11	Everolimus	16951235	CTD
12	Foscarnet	8384030	CTD
13	Hydrochlorothiazide	5823744	CTD
14	Ifosfamide	View details 2386379 2504390 2567921 8508598 8774570 8950339 9261752 11605785 16628552	CTD
15	Imatinib Mesylate	18215707	CTD
16	Irinotecan	19584382	CTD
17	Paroxetine	16958954	CTD
18	Phenytoin	6069279	CTD
19	Pyrazinamide	4340029	CTD
20	Sorafenib	19496710	CTD
21	Streptozocin	11219485	CTD
22	Theophylline	6506685	CTD
23	Valproic Acid	7624000 11891102 15785938	CTD
24	Vancomycin	17344665	CTD
25	Viomycin	4340029	CTD
26	adefovir dipivoxil	18815461	CTD
27	temsirolimus	20430774	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	31%
2	Calcium Metabolism Disorders	31%
3	Iron Metabolism Disorders	31%
4	Water-Electrolyte Imbalance	31%
5	Lipid Metabolism Disorders	31%
6	Mitochondrial Diseases	31%
7	Glucose Metabolism Disorders	31%
8	Wasting Syndrome	27.9%
9	Hypercalcemia	26.7%
10	Hypocalcemia	26.7%
11	Milk-Alkali Syndrome	26.7%
12	Osteopenia	20.9%
13	Brain Diseases, Metabolic	20.5%
14	Acidosis	20%
15	Alkalosis	20%
16	Amyloidosis	20%
17	Calcinosis	20%
18	Hyperglycemia	20%
19	Hyperinsulinism	20%
20	Hyperkalemia	20%
21	Hypernatremia	20%
22	Hypoglycemia	20%
23	Hypokalemia	20%
24	Hyponatremia	20%
25	Lipodystrophy	20%
26	Xanthomatosis	20%
27	Metabolic acidosis	20%
28	Dyslipidemias	20%
29	Iron Overload	20%
30	Xanthoma	20%
31	Nutrition Disorders	18.5%
32	Pseudohypoparathyroidism	18.1%
33	Rickets	17.3%
34	Brain Diseases, Metabolic, Inborn	15.9%
35	Leigh Disease	15.2%
36	Hyperhomocysteinemia	15.1%
37	Acidosis, Lactic	14.8%
38	Calciphylaxis	14.8%
39	Hemosiderosis	14.8%
40	Ketosis	14.8%
41	Ketonuria	14.8%
42	Ketoacidosis	14.8%
43	Ketonemia	14.8%
44	Vascular calcification	14.8%
45	Hypolipoproteinemias	14.6%
46	Hyperlipoproteinemia Type IV	14.5%
47	Hyperlipoproteinemia Type V	14.5%
48	Diabetes Mellitus	14.3%
49	Carbamoyl-Phosphate Synthase I Deficiency Disease	13.8%
50	Lactose Intolerance	13.7%
51	Dehydration	13.6%
52	Lipomatosis	13.6%
53	Water Intoxication	13.6%
54	Werner Syndrome	13.6%
55	Diabetic Ketoacidosis	13.5%
56	Hyperlipidemia, Familial Combined	13.4%
57	Achlorhydria	13.3%
58	Amino Acid Metabolism, Inborn Errors	13.3%
59	Bloom Syndrome	13.3%
60	Carbohydrate Metabolism, Inborn Errors	13.3%
61	Metal Metabolism, Inborn Errors	13.3%
62	Osteoporosis	13.3%
63	Progeria	13.3%
64	Lysosomal Storage Diseases	13.3%
65	Bone Demineralization, Pathologic	13.3%
66	Cytochrome-c Oxidase Deficiency	13.3%
67	Peroxisomal Disorders	13.3%
68	Post-Traumatic Osteoporosis	13.3%
69	Celiac Disease	13.2%
70	Sprue, Tropical	13.2%
71	Steatorrhea	13.2%
72	Sprue	13.2%
73	Osteomalacia	13%
74	Hyperlipoproteinemia Type III	12.7%
75	Smith-Lemli-Opitz Syndrome	12.6%
76	Galactosemias	12.5%
77	Urea Cycle Disorders, Inborn	12.5%
78	Tyrosinemias	12.5%
79	Hypercholesterolemia	12.2%
80	Hyperlipoproteinemias	12.2%
81	Hypertriglyceridemia	12.2%
82	Congenital Hyperinsulinism	12.2%
83	Hypoalphalipoproteinemias	12%
84	Mitochondrial Encephalomyopathies	11.5%
85	Gaucher Disease	10.9%
86	Glycogen storage disease type II	10.6%
87	Homocystinuria	10.4%
88	Child Nutrition Disorders	10.3%
89	Hypervitaminosis A	10.3%
90	Infant Nutrition Disorders	10.3%
91	Malnutrition	10.3%
92	Mitochondrial Myopathies	10.2%
93	Myelinolysis, Central Pontine	10.1%
94	Glycosuria	9.9%
95	Reye Syndrome	9.9%
96	Acidosis, Respiratory	9.9%
97	Adiposis Dolorosa	9.9%
98	Alkalosis, Respiratory	9.9%
99	Hepatic Encephalopathy	9.8%
100	Tay-Sachs Disease	9.8%
101	Nesidioblastosis	9.8%
102	Alkaptonuria	9.8%
103	Glycogen Storage Disease	9.8%
104	Hypophosphatasia	9.8%
105	Insulin Resistance	9.8%
106	Osteoporosis, Postmenopausal	9.8%
107	Propionic acidemia	9.8%
108	Dihydropyrimidine Dehydrogenase Deficiency	9.8%
109	Cystinosis	9.8%
110	Amyloid Neuropathies, Familial	9.8%
111	Renal tubular acidosis	9.7%
112	Niemann-Pick Disease, Type C	9.3%
113	Neuronal Ceroid-Lipofuscinoses	9%
114	HIV Wasting Syndrome	8.8%
115	Fabry Disease	8.5%
116	HIV-Associated Lipodystrophy Syndrome	8.4%
117	MELAS Syndrome	8.2%
118	Renal Osteodystrophy	8.2%
119	Renal rickets	8.2%
120	Porphyrias, Hepatic	8.1%
121	Glycogen Storage Disease Type I	8.1%
122	Glycogen Storage Disease Type V	8.1%
123	Zellweger Syndrome	8%
124	Mucopolysaccharidosis III	8%
125	Adrenoleukodystrophy	8%
126	Necrobiosis Lipoidica Diabeticorum	7.9%
127	Menkes Kinky Hair Syndrome	7.9%
128	Familial Hypophosphatemic Rickets	7.8%
129	Fanconi Anemia	7.8%
130	Wernicke Encephalopathy	7.7%
131	Gestational Diabetes	7.7%
132	Latent Autoimmune Diabetes in Adults	7.7%
133	Diabetes Mellitus, Experimental	7.6%
134	Hepatolenticular Degeneration	7.4%
135	Nephrocalcinosis	7.4%
136	Tetany	7.4%
137	Refsum Disease	7.3%
138	Hyperphosphaturia	7.3%
139	Glycosuria, Renal	7.3%
140	Cerebral Amyloid Angiopathy	7.2%
141	Deficiency Diseases	6.7%
142	Starvation	6.7%
143	Refeeding Syndrome	6.7%
144	Friedreich Ataxia	6.5%
145	Familial Periodic Paralysis	6%
146	Primary amyloidosis	6%
147	Variegate Porphyria	5.9%
148	Acute intermittent porphyria	5.9%
149	Porphyria Cutanea Tarda	5.9%
150	Renal Aminoacidurias	5.8%
151	Fanconi Syndrome	5.8%
152	Pseudohypoaldosteronism	5.8%
153	Liddle Syndrome	5.8%
154	Kernicterus	5.7%
155	Kearns-Sayre syndrome	5.7%
156	Cockayne Syndrome	5.7%
157	Canavan Disease	5.4%
158	Alexander Disease	5.4%
159	Sjogren-Larsson Syndrome	5.4%
160	Mucopolysaccharidosis II	5.3%
161	Ataxia Telangiectasia	5.1%
162	Gout	5%
163	Amyotrophic Lateral Sclerosis	5%
164	Kwashiorkor	4.9%
165	Magnesium Deficiency	4.9%
166	Potassium Deficiency	4.9%
167	Protein Deficiency	4.9%
168	Avitaminosis	4.9%
169	Optic Atrophy, Hereditary, Leber	4.9%
170	Antley-Bixler Syndrome Phenotype	4.9%
171	Hypokalemic periodic paralysis	4.9%
172	Frontotemporal dementia	4.8%
173	Cystinuria	4.8%
174	Xeroderma Pigmentosum	4.5%
175	CREST Syndrome	4.2%
176	Ascorbic Acid Deficiency	4.1%
177	Vitamin A Deficiency	4.1%
178	Vitamin D Deficiency	4.1%
179	Vitamin E Deficiency	4.1%
180	Marasmus	4.1%
181	Arthritis, Gouty	4.1%
182	Albinism	3.7%
183	Folic Acid Deficiency	3.6%
184	Pellagra	3.6%
185	Thiamine Deficiency	3.6%
186	Vitamin B 12 Deficiency	3.6%
187	Vitamin B 6 Deficiency	3.6%
188	Pyridoxine Deficiency	3.6%
189	Beriberi	3.4%
190	Ichthyosis, X-Linked	3%
191	Obesity	2.6%
192	Obesity, Abdominal	2.4%
193	Anemia, Pernicious	2.3%
194	Vitamin K Deficiency	2.1%
195	Pediatric Obesity	1.9%
196	Scurvy	1.8%
197	Prader-Willi Syndrome	1.6%
198	Subacute Combined Degeneration	1.2%

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