MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Phosphorus Metabolism Disorders

(UMLS:C0031707)

Definition:: Disorders in the processing of phosphorus in the body: its absorption, transport, storage, and utilization.
UMLS ID:: C0031707
MeSH ID:: D010760

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.750

Synonym(s)

Phosphorus Metabolism Disorders

Disorder of phosphorus metabolism

Disorder of phosphorus metabolism, NOS

Disorders of phosphorus metabolism

Phosphorus Metabolic Disorder

Phosphorus metabolism disorder

Phosphorus--Metabolism--Disorders

metabolic disorder; phosphorus

phosphorus metabolism disorder

10.

phosphorus; metabolic disorder

Associated Drug(s)

	Name	Reference(s)	Data Source
1	Calcitriol	6688127	CTD
2	PD 0325901	21976371	CTD
3	Phosphorus	21976371	CTD

Similar ADE(s)

	Name	Semantic Similarity
1	Acid-Base Imbalance	42.9%
2	Calcium Metabolism Disorders	42.9%
3	Iron Metabolism Disorders	42.9%
4	Water-Electrolyte Imbalance	42.9%
5	Lipid Metabolism Disorders	42.9%
6	Mitochondrial Diseases	42.9%
7	Glucose Metabolism Disorders	42.9%
8	Hypercalcemia	40.9%
9	Hypocalcemia	40.9%
10	Milk-Alkali Syndrome	40.9%
11	Wasting Syndrome	38.1%
12	Acidosis	31%
13	Alkalosis	31%
14	Amyloidosis	31%
15	Calcinosis	31%
16	Hyperglycemia	31%
17	Hyperinsulinism	31%
18	Hyperkalemia	31%
19	Hypernatremia	31%
20	Hypoglycemia	31%
21	Hypokalemia	31%
22	Hyponatremia	31%
23	Xanthomatosis	31%
24	Metabolic acidosis	31%
25	Dyslipidemias	31%
26	Iron Overload	31%
27	Xanthoma	31%
28	Lipodystrophy	30.5%
29	Osteopenia	28.6%
30	Pseudohypoparathyroidism	28.3%
31	Brain Diseases, Metabolic	27.9%
32	Rickets	26.9%
33	Hyperlipoproteinemia Type IV	26.4%
34	Hyperlipoproteinemia Type V	26.4%
35	Acidosis, Lactic	25.4%
36	Calciphylaxis	25.4%
37	Hemosiderosis	25.4%
38	Ketosis	25.4%
39	Ketonuria	25.4%
40	Ketoacidosis	25.4%
41	Ketonemia	25.4%
42	Vascular calcification	25.4%
43	Leigh Disease	25.1%
44	Hypolipoproteinemias	24.8%
45	Hyperhomocysteinemia	24.5%
46	Brain Diseases, Metabolic, Inborn	24.2%
47	Carbamoyl-Phosphate Synthase I Deficiency Disease	23.7%
48	Diabetic Ketoacidosis	23.7%
49	Hyperlipidemia, Familial Combined	23.5%
50	Nutrition Disorders	23.1%
51	Hyperlipoproteinemia Type III	22.8%
52	Hypercholesterolemia	22.7%
53	Hyperlipoproteinemias	22.7%
54	Hypertriglyceridemia	22.7%
55	Osteomalacia	22.3%
56	Hypoalphalipoproteinemias	22%
57	Diabetes Mellitus	22%
58	Lactose Intolerance	21.9%
59	Smith-Lemli-Opitz Syndrome	21.1%
60	Galactosemias	21%
61	Urea Cycle Disorders, Inborn	21%
62	Tyrosinemias	21%
63	Dehydration	20.9%
64	Lipomatosis	20.9%
65	Water Intoxication	20.9%
66	Werner Syndrome	20.9%
67	Gaucher Disease	20.6%
68	Congenital Hyperinsulinism	20.5%
69	Achlorhydria	20.5%
70	Amino Acid Metabolism, Inborn Errors	20.5%
71	Bloom Syndrome	20.5%
72	Carbohydrate Metabolism, Inborn Errors	20.5%
73	Metal Metabolism, Inborn Errors	20.5%
74	Osteoporosis	20.5%
75	Progeria	20.5%
76	Lysosomal Storage Diseases	20.5%
77	Bone Demineralization, Pathologic	20.5%
78	Cytochrome-c Oxidase Deficiency	20.5%
79	Peroxisomal Disorders	20.5%
80	Post-Traumatic Osteoporosis	20.5%
81	Celiac Disease	20.2%
82	Sprue, Tropical	20.2%
83	Steatorrhea	20.2%
84	Sprue	20.2%
85	Tay-Sachs Disease	19.4%
86	Glycogen storage disease type II	19.3%
87	Mitochondrial Encephalomyopathies	18.2%
88	Niemann-Pick Disease, Type C	18%
89	Nesidioblastosis	17.9%
90	Homocystinuria	17.9%
91	Amyloid Neuropathies, Familial	17.2%
92	Acidosis, Respiratory	16.9%
93	Adiposis Dolorosa	16.9%
94	Alkalosis, Respiratory	16.9%
95	Alkaptonuria	16.7%
96	Glycogen Storage Disease	16.7%
97	Hypophosphatasia	16.7%
98	Insulin Resistance	16.7%
99	Osteoporosis, Postmenopausal	16.7%
100	Propionic acidemia	16.7%
101	Dihydropyrimidine Dehydrogenase Deficiency	16.7%
102	Cystinosis	16.7%
103	Renal tubular acidosis	16.3%
104	Fabry Disease	15.9%
105	Neuronal Ceroid-Lipofuscinoses	15.7%
106	Mitochondrial Myopathies	15.5%
107	Myelinolysis, Central Pontine	15.4%
108	Glycosuria	15.1%
109	Reye Syndrome	15.1%
110	Hepatic Encephalopathy	15%
111	Glycogen Storage Disease Type I	14.8%
112	Glycogen Storage Disease Type V	14.8%
113	Mucopolysaccharidosis III	14.6%
114	Child Nutrition Disorders	14.3%
115	Hypervitaminosis A	14.3%
116	Infant Nutrition Disorders	14.3%
117	Malnutrition	14.3%
118	Familial Hypophosphatemic Rickets	14.3%
119	MELAS Syndrome	14.1%
120	HIV-Associated Lipodystrophy Syndrome	14.1%
121	Renal Osteodystrophy	13.9%
122	Renal rickets	13.9%
123	Adrenoleukodystrophy	13.7%
124	Zellweger Syndrome	13.5%
125	Menkes Kinky Hair Syndrome	13.3%
126	HIV Wasting Syndrome	13.3%
127	Gestational Diabetes	13%
128	Latent Autoimmune Diabetes in Adults	13%
129	Diabetes Mellitus, Experimental	12.8%
130	Nephrocalcinosis	12.5%
131	Tetany	12.5%
132	Hepatolenticular Degeneration	12.4%
133	Porphyrias, Hepatic	12.3%
134	Cerebral Amyloid Angiopathy	12.3%
135	Wernicke Encephalopathy	12.2%
136	Hyperphosphaturia	12.2%
137	Glycosuria, Renal	12.2%
138	Refsum Disease	12.2%
139	Necrobiosis Lipoidica Diabeticorum	12.1%
140	Fanconi Anemia	11.9%
141	Deficiency Diseases	10.3%
142	Starvation	10.3%
143	Refeeding Syndrome	10.3%
144	Familial Periodic Paralysis	10.1%
145	Primary amyloidosis	10.1%
146	Variegate Porphyria	9.9%
147	Acute intermittent porphyria	9.9%
148	Porphyria Cutanea Tarda	9.9%
149	Friedreich Ataxia	9.9%
150	Renal Aminoacidurias	9.8%
151	Fanconi Syndrome	9.8%
152	Pseudohypoaldosteronism	9.8%
153	Liddle Syndrome	9.8%
154	Canavan Disease	9.8%
155	Alexander Disease	9.8%
156	Mucopolysaccharidosis II	9.7%
157	Sjogren-Larsson Syndrome	9.3%
158	Kearns-Sayre syndrome	9.3%
159	Hypokalemic periodic paralysis	8.9%
160	Frontotemporal dementia	8.8%
161	Cystinuria	8.8%
162	Kernicterus	8.7%
163	Cockayne Syndrome	8.6%
164	Kwashiorkor	8.5%
165	Magnesium Deficiency	8.5%
166	Potassium Deficiency	8.5%
167	Protein Deficiency	8.5%
168	Avitaminosis	8.5%
169	Gout	8.4%
170	Amyotrophic Lateral Sclerosis	8.4%
171	Antley-Bixler Syndrome Phenotype	8.2%
172	Ataxia Telangiectasia	7.6%
173	Ascorbic Acid Deficiency	7.6%
174	Vitamin A Deficiency	7.6%
175	Vitamin D Deficiency	7.6%
176	Vitamin E Deficiency	7.6%
177	Marasmus	7.6%
178	Optic Atrophy, Hereditary, Leber	7.4%
179	Arthritis, Gouty	7.4%
180	Folic Acid Deficiency	7.1%
181	Pellagra	7.1%
182	Thiamine Deficiency	7.1%
183	Vitamin B 12 Deficiency	7.1%
184	Vitamin B 6 Deficiency	7.1%
185	Pyridoxine Deficiency	7.1%
186	CREST Syndrome	7%
187	Beriberi	6.9%
188	Xeroderma Pigmentosum	6.8%
189	Albinism	6.3%
190	Ichthyosis, X-Linked	5%
191	Anemia, Pernicious	4.5%
192	Obesity, Abdominal	4.1%
193	Obesity	3.9%
194	Vitamin K Deficiency	3.8%
195	Scurvy	3.5%
196	Pediatric Obesity	3.2%
197	Prader-Willi Syndrome	2.8%
198	Subacute Combined Degeneration	2.3%

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