Hereditary coproporphyria
... (HCP) is a disorder of heme biosynthesis, classified as an acute hepatic porphyria. HCP is caused by ... 121300 COPROPORPHYRIA, HEREDITARY; HCP". Johns Hopkins University. Retrieved 2012-05-27. Tortorelli, Silvia; Kloke, Karen M.; ... "Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic ... Porphyria at NLM Genetics Home Reference Coproporphyria at NIH's Office of Rare Diseases MedlinePlus Encyclopedia: Porphyria ( ...
Coproporphyrinogen III oxidase
Hereditary coproporphyria (HCP) and harderoporphyria are two phenotypically separate disorders that concern partial deficiency ... The medical condition associated with this enzyme defect is called hereditary coproporphyria. CPOX, the sixth enzyme of the ... Martasek P, Nordmann Y, Grandchamp B (March 1994). "Homozygous hereditary coproporphyria caused by an arginine to tryptophane ... Martasek P, Nordmann Y, Grandchamp B (March 1994). "Homozygous hereditary coproporphyria caused by an arginine to tryptophane ...
Aminolevulinic acid dehydratase deficiency porphyria
"Hereditary Coproporphyria". GeneReviews. PMID 23236641. Retrieved 28 February 2020. the symptoms in lead poisoning closely ...
Porphyria
Hereditary coproporphyria, which is characterized by a deficiency in coproporphyrinogen oxidase, coded for by the CPOX gene, ... The exception to this may be latent post-puberty genetic carriers of hereditary coproporphyria.[citation needed] As most ... hereditary coproporphyria, variegate porphyria) have been noted in DNA tests to be latent for classic symptoms and may require ... and hereditary coproporphyria (HCP). These diseases primarily affect the nervous system, resulting in episodic crises known as ...
Lead poisoning
"Hereditary Coproporphyria". GeneReviews. PMID 23236641. Retrieved 28 February 2020. the symptoms in lead poisoning closely ...
Polymorphous light eruption
Variegate porphyria and hereditary coproporphyria can also exhibit symptoms of light-induced blisters. Sunlight has been ... "Hereditary Coproporphyria (HCP)". American Porphyria Foundation. 18 February 2009. Retrieved 4 June 2018. Rapini RP, Bolognia ... Actinic Prurigo is a hereditary form of PLE occurring typically in Native Americans. Management entails regulating triggers ...
Harderoporphyria
121300 COPROPORPHYRIA, HEREDITARY; HCP". Johns Hopkins University. Retrieved 2012-05-27. Gorchein, A.; Danton, M.; Lim, C. K. ( ... Mutations in CPOX usually cause hereditary coproporphyria, an acute hepatic porphyria, however the K404E mutation in a ... A variant hereditary coproporphyria". Journal of Clinical Investigation. 72 (3): 1139-1149. doi:10.1172/JCI111039. PMC 1129282 ... "Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic ...
Acute intermittent porphyria
Elevated urine porphobilinogen confirms diagnosis of AIP, hereditary coproporphyria (HCP), or variegate porphyria (VP). A ...
Hepatoerythropoietic porphyria
Hereditary coproporphyria List of cutaneous conditions List of dental abnormalities associated with cutaneous conditions " ...
Hives
Dominantly inherited cutaneous and neurocutaneous porphyrias (porphyria cutanea tarda, hereditary coproporphyria, variegate ... The rare form is hereditary and becomes evident as hives all over the body 9 to 18 hours after cold exposure. The common form ...
Alcohol and cancer
... variegate porphyria and hereditary coproporphyria. Porphyria cutanea tarda is also associated with HCC, but with typical risk ...
Hepatocellular carcinoma
... hereditary coproporphyria, variegate porphyria) and tyrosinemia type I are risk factors for hepatocellular carcinoma. The ...
Hepatic porphyria
Acute intermittent porphyria Porphyria cutanea tarda and Hepatoerythropoietic porphyria Hereditary coproporphyria Variegate ...
Heme
... hereditary coproporphyria, variegate porphyria, erythropoietic protoporphyria.[citation needed] Impossible Foods, producers of ... deficiency causes hereditary coproporphyria) FECH: ferrochelatase (deficiency causes erythropoietic protoporphyria) HMBS: ...
Psychomotor agitation
Hereditary coproporphyria Variegate porphyria Side effects of drugs like cocaine or methylphenidate Side effects of ...
HCP
... a venture capital firm Healthcare professional Hereditary coproporphyria Himalayan Cataract Project Human Connectome Project ...
Chromosome 3
... progressive/nonprogressive Hereditary coproporphyria Hereditary nonpolyposis colorectal cancer HIV infection, susceptibility/ ... hereditary motor and sensory, Okinawa type Night blindness Nonsyndromic deafness Ovarian cancer Porphyria Propionic acidemia ... coproporphyria, harderoporphyria) DPPA2: Developmental pluripotency associated 2 DTX3L: encoding protein Deltex e3 ubiquitin ... type 2 Charcot-Marie-Tooth disease Chromosome 3q duplication syndrome Coproporphyria A location on human chromosome 3 is ...
List of MeSH codes (C06)
... coproporphyria, hereditary MeSH C06.552.830.150 - porphyria, acute intermittent MeSH C06.552.830.250 - porphyria cutanea tarda ... hereditary nonpolyposis MeSH C06.301.371.411.307.790 - rectal neoplasms MeSH C06.301.371.411.307.790.040 - anus neoplasms MeSH ... hereditary nonpolyposis MeSH C06.405.249.411.307.790 - rectal neoplasms MeSH C06.405.249.411.307.790.040 - anus neoplasms MeSH ... hereditary nonpolyposis MeSH C06.405.469.491.307.790 - rectal neoplasms MeSH C06.405.469.491.307.790.040 - anus neoplasms MeSH ...
Dysuria
Diverticulitis Hypotension Mass in the abdomen Reactive arthritis Acute intermittent porphyria Hereditary coproporphyria ...
Syndrome of inappropriate antidiuretic hormone secretion
... hereditary coproporphyria, variegate porphyria) Multiple system atrophy Multiple sclerosis Cancers Carcinomas Lung cancers ( ... Oxytocin Vincristine Morphine Amitriptyline Transient causes Endurance exercise General anesthesia Hereditary causes ...
List of MeSH codes (C18)
... coproporphyria, hereditary MeSH C18.452.648.735.150 - porphyria, acute intermittent MeSH C18.452.648.735.250 - porphyria ... coproporphyria, hereditary MeSH C18.452.872.617.400.150 - porphyria, acute intermittent MeSH C18.452.872.617.400.250 - ... hereditary nonpolyposis MeSH C18.452.284.280 - fanconi anemia MeSH C18.452.284.520 - Li-Fraumeni syndrome MeSH C18.452.284.600 ... hereditary MeSH C18.452.648.437.281 - Crigler-Najjar syndrome MeSH C18.452.648.437.528 - gilbert disease MeSH C18.452.648.499 ...
List of MeSH codes (C16)
... coproporphyria, hereditary MeSH C16.320.565.735.150 - porphyria, acute intermittent MeSH C16.320.565.735.250 - porphyria ... coproporphyria, hereditary MeSH C16.320.850.742.150 - porphyria, acute intermittent MeSH C16.320.850.742.250 - porphyria ... hereditary MeSH C16.320.290.564.400 - optic atrophy, hereditary, leber MeSH C16.320.290.564.500 - optic atrophy, autosomal ... hereditary central nervous system demyelinating diseases MeSH C16.320.400.400 - hereditary motor and sensory neuropathies MeSH ...
List of diseases (H)
Hereditary coproporphyria Hereditary deafness Hereditary elliptocytosis Hereditary fibrinogen Aα-Chain amyloidosis Hereditary ... Hereditary m Hereditary amyloidosis Hereditary angioedema Hereditary ataxia Hereditary carnitine deficiency myopathy Hereditary ... Hereditary t Hereditary nodular heterotopia Hereditary non-spherocytic hemolytic anemia Hereditary pancreatitis Hereditary ... Hereditary hearing disorder Hereditary hearing loss Hereditary hemochromatosis Hereditary hemorrhagic telangiectasia Hereditary ...
List of diseases (P)
... hereditary coproporphyria Portal hypertension due to intrahepatic block Portal hypertension Portal thrombosis Portal vein ... hereditary Pancreatoblastoma Panhypopituitarism Panic disorder Panmyelophthisis aplastic anemia Panniculitis Panophobia ... POEMS syndrome Poedimus kyleopecia mental retardation Poikiloderma congenital with bullae Weary type Poikiloderma hereditary ...
List of MeSH codes (C17)
... coproporphyria, hereditary MeSH C17.800.827.742.150 - porphyria, acute intermittent MeSH C17.800.827.742.250 - porphyria ... coproporphyria, hereditary MeSH C17.800.849.617.400.150 - porphyria, acute intermittent MeSH C17.800.849.617.400.250 - ...
List of OMIM disorder codes
... hereditary, type III; 610618; F12 Angioedema, hereditary, types I and II; 106100; C1NH Angiopathy, hereditary, with nephropathy ... MMP1 Coproporphyria; 121300; CPOX Cornea plana congenita, recessive; 217300; KERA Corneal dystrophy polymorphous posterior, 2; ... ENG Hereditary hemorrhagic telangiectasia-2; 600376; ACVRL1 Hereditary motor and sensory neuropathy VI; 601152; MFN2 Hereditary ... distal hereditary motor, type IIB; 608634; HSPB1 Neuropathy, distal hereditary motor, type V; 600794; BSCL2 Neuropathy, distal ...
List of skin conditions
Hemodialysis-associated amyloidosis Hepatoerythropoietic porphyria Hereditary coproporphyria Hereditary gelsolin amyloidosis ... hereditary painful callosities, hereditary painful callosity syndrome, keratosis follicularis, keratosis palmoplantaris ... Centola M, Aksentijevich I, Kastner DL (1998). "The hereditary periodic fever syndromes: molecular analysis of a new family of ... Fietta P (2004). "Autoinflammatory diseases: the hereditary periodic fever syndromes". Acta Biomed. 75 (2): 92-9. PMID 15481697 ...