serw-MX  [xml]  

 DeCS Categories

B01 Eukaryota .
B01.650 Plants .
B01.650.700 Rhodophyta .
B01.650.700.600 Porphyra .
B01.650.700.610 Porphyridium .
B03 Bacteria .
B03.140 Bacteroidetes .
B03.140.094 Bacteroidaceae .
B03.140.094.625 Porphyromonas .
B03.440 Gram-Negative Bacteria .
B03.440.425 Gram-Negative Anaerobic Bacteria .
B03.440.425.410 Gram-Negative Anaerobic Straight, Curved, and Helical Rods .
B03.440.425.410.194 Bacteroidaceae .
B03.440.425.410.194.625 Porphyromonas .
C06 Digestive System Diseases .
C06.552 Liver Diseases .
C06.552.830 Porphyrias, Hepatic .
C06.552.830.150 Porphyria, Acute Intermittent .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.742 Porphyrias, Hepatic .
C16.320.850.742.150 Porphyria, Acute Intermittent .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.742 Porphyrias, Hepatic .
C17.800.827.742.150 Porphyria, Acute Intermittent .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.811 Porphyrias .
C18.452.811.400 Porphyrias, Hepatic .
C18.452.811.400.150 Porphyria, Acute Intermittent .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.129 Azoles .
D03.383.129.578 Pyrroles .
D03.383.129.578.840 Tetrapyrroles .
D03.383.129.578.840.500 Porphyrins .
D03.383.129.578.840.500.700 Porphyrinogens .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.400 Heterocyclic Compounds, 4 or More Rings .
D03.633.400.909 Tetrapyrroles .
D03.633.400.909.500 Porphyrins .
D03.633.400.909.500.700 Porphyrinogens .
D04 Polycyclic Compounds .
D04.345 Macrocyclic Compounds .
D04.345.783 Tetrapyrroles .
D04.345.783.500 Porphyrins .
D04.345.783.500.700 Porphyrinogens .
D23 Biological Factors .
D23.767 Pigments, Biological .
D23.767.727 Porphyrins .
 Synonyms & Historicals
Porphyra .
Norus .
Porphyras .
Nori 25464 .
A genus of RED ALGAE in the family Bangiaceae. It is the most widely consumed SEAWEED in the world and especially in Asia. .
Porphyrias .
Porphyria .
Porphyrin Disorder .
Disorder, Porphyrin .
Disorders, Porphyrin .
Porphyrin Disorders .
A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues. .
Porphyrins .
A group of compounds containing the porphin structure, four pyrrole rings connected by methine bridges in a cyclic configuration to which a variety of side chains are attached. The nature of the side chain is indicated by a prefix, as uroporphyrin, hematoporphyrin, etc. The porphyrins, in combination with iron, form the heme component in biologically significant compounds such as hemoglobin and myoglobin. .
Porphyridium .
Porphyridiums .
A genus of RED ALGAE in the family Porphyridiaceae. A single stellate CHLOROPLAST is present in each cell which has no CELL WALL. .
Porphyromonas .
A genus of gram-negative, anaerobic, nonsporeforming, nonmotile rods or coccobacilli. Organisms in this genus had originally been classified as members of the BACTEROIDES genus but overwhelming biochemical and chemical findings indicated the need to separate them from other Bacteroides species, and hence, this new genus was created. .
Porphyrinogens .
Colorless reduced precursors of porphyrins in which the pyrrole rings are linked by methylene (-CH2-) bridges. .
Porphyria, Acute Intermittent .
Acute Porphyria .
PBGD Deficiency .
Porphobilinogen Deaminase Deficiency .
Porphyria, Swedish Type .
UPS Deficiency .
Acute Intermittent Porphyria .
Acute Intermittent Porphyrias .
Acute Porphyrias .
Deaminase Deficiencies, Porphobilinogen .
Deaminase Deficiency, Porphobilinogen .
Deficiencies, Hydroxymethylbilane Synthase .
Deficiencies, PBGD .
Deficiencies, Porphobilinogen Deaminase .
Deficiencies, UPS .
Deficiencies, Uroporphyrinogen Synthase .
Deficiency, Hydroxymethylbilane Synthase .
Deficiency, PBGD .
Deficiency, Porphobilinogen Deaminase .
Deficiency, UPS .
Deficiency, Uroporphyrinogen Synthase .
Hydroxymethylbilane Synthase Deficiencies .
Intermittent Porphyria, Acute .
Intermittent Porphyrias, Acute .
PBGD Deficiencies .
Porphobilinogen Deaminase Deficiencies .
Porphyria, Acute .
Porphyrias, Acute .
Porphyrias, Acute Intermittent .
Porphyrias, Swedish Type .
Swedish Type Porphyria .
Swedish Type Porphyrias .
Synthase Deficiencies, Hydroxymethylbilane .
Synthase Deficiencies, Uroporphyrinogen .
Synthase Deficiency, Hydroxymethylbilane .
Synthase Deficiency, Uroporphyrinogen .
Type Porphyria, Swedish .
Type Porphyrias, Swedish .
UPS Deficiencies .
Uroporphyrinogen Synthase Deficiencies .
Hydroxymethylbilane Synthase Deficiency .
Uroporphyrinogen Synthase Deficiency .
An autosomal dominant porphyria that is due to a deficiency of HYDROXYMETHYLBILANE SYNTHASE in the LIVER, the third enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features are recurrent and life-threatening neurologic disturbances, ABDOMINAL PAIN, and elevated level of AMINOLEVULINIC ACID and PORPHOBILINOGEN in the urine. .