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hereditary coproporphyria - multisystem disease due to abnormality in heme metabolism
Definition for hereditary coproporphyria
Hereditary coproporphyria (HCP) is a form of hepatic porphyria associated with a deficiency of the enzyme coproporphyrinogen III oxidase.
some common symptoms
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do i have 'hereditary coproporphyria'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'hereditary coproporphyria'
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Stool coproporphyrins
hereditary coproporphyria and Stool coproporphyrins
Complete metabolic panel
hereditary coproporphyria and Complete metabolic panel
Urine coproporphyrins
hereditary coproporphyria and Urine coproporphyrins
Blood, Platelet Count
Platelet Count
hereditary coproporphyria and Blood, Platelet Count
Complete Blood Count
hereditary coproporphyria and Complete Blood Count
Liver Function Tests
elevated liver enzymes
hereditary coproporphyria and Liver Function Tests
Trace PBG Kit
hereditary coproporphyria and Trace PBG Kit
serum electrolytes
hereditary coproporphyria and serum electrolytes
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therapeutic procedures for 'hereditary coproporphyria'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for hereditary coproporphyria:
therapeutic procedure search results for 'hereditary coproporphyria'
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high-carbohydrate diet
hereditary coproporphyria and high-carbohydrate diet
Sun protection
hereditary coproporphyria and Sun protection
Intravenous (IV) glucose
hereditary coproporphyria and Intravenous (IV) glucose
Nutritional counseling
hereditary coproporphyria and Nutritional counseling
diet modification
hereditary coproporphyria and diet modification
medications search results for 'hereditary coproporphyria'
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Panhematin
hereditary coproporphyria and Panhematin
web search results for hereditary coproporphyria
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- hereditary coproporphyria
Hereditary coproporphyria - Wikipedia, the free encyclopedia
Hereditary coproporphyria (HCP) is a form of hepatic porphyria associated with a ... Hereditary coproporphyria is the result of a point mutation in the ...
http://en.wikipedia.org/wiki/Hereditary_coproporphyria
en.wikipedia.org
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summary
Homozygous hereditary coproporphyria caused by an arginine to ...
Homozygous hereditary coproporphyria caused by an arginine to tryptophane ... of this enzyme causes the human genetic disease hereditary coproporphyria. ...
http://www.ncbi.nlm.nih.gov/pubmed/8012360
www.ncbi.nlm.nih.gov
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summary
Hereditary coproporphyria: exon screening by heteroduplex analysis ...
Hereditary coproporphyria: exon screening by heteroduplex analysis detects three ... Hereditary coproporphyria is a dominantly inherited disorder of porphyrin ...
http://www.ncbi.nlm.nih.gov/pubmed/9298818
www.ncbi.nlm.nih.gov
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summary
Porphyria, Hereditary Coproporphyria - Yahoo! Health
Important It is possible that the main title of the report Porphyria, Hereditary Coproporphyria is not the name you expected. Please check the synonyms listing to ...
http://health.yahoo.com/children-genetic/porphyria-hereditar...
health.yahoo.com
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summary
Porphyria
Porphyrias are a rare group of disorders passed down through families in which ... intermittent porphyria; Hereditary coproporphyria; Congenital erythropoietic ...
http://adam.about.com/encyclopedia/infectiousdiseases/Porphyria_1.htm
adam.about.com
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summary
Porphyria - Genetics Home Reference
... hepatoerythropoietic porphyria, hereditary coproporphyria, porphyria cutanea ... form of the disorder, hereditary coproporphyria, has been reported mostly in ...
http://ghr.nlm.nih.gov/condition=hereditarycoproporphyria
ghr.nlm.nih.gov
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summary
MedlinePlus Medical Encyclopedia: Porphyria
... intermittent porphyria; Hereditary coproporphyria; Congenital erythropoietic ... Porphyrias are a rare group of disorders passed down through families in which ...
http://www.nlm.nih.gov/medlineplus/ency/article/001208.htm
www.nlm.nih.gov
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summary
Health Library - Avera Health
Porphyrias are a rare group of disorders passed down through families in which ... intermittent porphyria; Hereditary coproporphyria; Congenital erythropoietic ...
http://averaorg.adam.com/content.aspx?productId=101&pid=1&gid=001208
averaorg.adam.com
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summary
Acute Porphyrias: Porphyrias: Merck Manual Professional
... variegate porphyria and hereditary coproporphyria may develop bullous eruptions ... hereditary coproporphyria (HCP), and the exceedingly rare ? ...
http://www.merck.com/mmpe/print/sec12/ch155/ch155b.html
www.merck.com
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summary
Health Information - MMCI
MMCI - Methodist Medical Center, methodist hospital, Illinois hospital, peoria hospital ... Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ...
http://mmci2.adam.com/content.aspx?productId=101&alpha=H&sub=Disease
mmci2.adam.com
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summary
Table of Contents: Medicine, Ob/Gyn, Psychiatry, and Surgery
emedicine features up-to-date, searchable, peer-reviewed medical journals in emergency medicine, internal medicine, ... Hereditary Coproporphyria. Protein ...
http://author.emedicine.com/med/HEMATOLOGY.htm
author.emedicine.com
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CPOX - References - Genetics Home Reference
... of hereditary coproporphyria. ... defects in hereditary coproporphyria and mutation ... either hepatic hereditary coproporphyria or erythropoietic ...
http://ghr.nlm.nih.gov/gene=cpox/show/References
ghr.nlm.nih.gov
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summary
Identification of a novel mutation of the CPO gene in a Japanese ...
... mutation of the CPO gene in a Japanese hereditary coproporphyria family. ... Hereditary coproporphyria (HCP) is an autosomal dominant disease characterized ...
http://www.ncbi.nlm.nih.gov/pubmed/9843038
www.ncbi.nlm.nih.gov
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summary
adam.about.com
Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ... Hereditary sensory and autonomic neuropathy - type III (HSAN III) Hereditary ...
http://adam.about.com/encyclopedia/diseidxh.htm
adam.about.com
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summary
Health Library - Avera Health
Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ... Hereditary sensory and autonomic neuropathy - type III (HSAN III) Hereditary ...
http://averaorg.adam.com/content.aspx?productId=101&alpha=H&sub=Disease
averaorg.adam.com
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summary
Cutaneous Porphyrias: Porphyrias: Merck Manual Professional
... variegate porphyria and hereditary coproporphyria also have cutaneous manifestations. ... mutation is sporadic; the remaining 20% are hereditary. ...
http://www.merck.com/mmpe/print/sec12/ch155/ch155c.html
www.merck.com
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summary
emailAFriend
Porphyria, Hereditary Coproporphyria * Indicates required fields. From: Your Name: ... Clicking the send button signifies that you have read and agree to our ...
http://www.webmd.com/email_friend?chronicID=091e9c5e8001ec46
www.webmd.com
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summary
MedlinePlus Medical Encyclopedia: Topics beginning with H-Hf
Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria see Porphyria ... Hereditary hemorrhagic telangiectasia see Osler-Weber-Rendu syndrome ...
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_H-Hf.htm
www.nlm.nih.gov
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Systematic analysis of coproporphyrinogen oxidase gene defects in ...
... oxidase gene defects in hereditary coproporphyria and mutation update. ... Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal ...
http://www.ncbi.nlm.nih.gov/pubmed/9888388
www.ncbi.nlm.nih.gov
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summary
JPMC Online | Health Encyclopedia
Providing excellence in healthcare in Bartlesville, Oklahoma. ... Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ...
http://jpmc.adam.com/content.aspx?productId=101&alpha=H
jpmc.adam.com
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summary
Health Information
A member of SSM Health Care. Body, Mind, Spirit... We care for the whole person. ... Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ...
http://ssmhealth.adam.com/content.aspx?pid=1&gid=200000&sub=Disease&alpha=H
ssmhealth.adam.com
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summary
Disease Reference
Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ... Hereditary urea cycle abnormality. Hermaphrodite. Hermaphroditism. Hernia. Hernia ...
http://adam.about.com/HIE/diseidxh.htm
adam.about.com
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summary
CPOX - coproporphyrinogen oxidase - Genetics Home Reference
... than 35 mutations that cause hereditary coproporphyria (a type of porphyria) and ... coproporphyrinogen oxidase (coproporphyria, harderoporphyria) ...
http://ghr.nlm.nih.gov/gene=cpox
ghr.nlm.nih.gov
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summary
Characterization of mutations in the CPO gene in British patients ...
... identifies relationship between hereditary coproporphyria and harderoporphyria. ... Hereditary coproporphyria (HCP) is the least common of the autosomal dominant ...
http://www.ncbi.nlm.nih.gov/pubmed/11309681
www.ncbi.nlm.nih.gov
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summary
Porphyria
Important It is possible that the main title of the report Porphyria is not the ... Hereditary Coproporphyria. Protoporphyria. Porphyria Cutanea Tarda ...
http://www.webmd.com/a-to-z-guides/porphyria-10646
www.webmd.com
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summary
Introduction: Porphyrias: Merck Manual Home Edition
Introduction· Acute Intermittent Porphyria· Erythropoietic Protoporphyria ... include variegate porphyria, hereditary coproporphyria, and the extremely rare ...
http://www.merck.com/mmhe/sec12/ch160/ch160a.html
www.merck.com
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summary
Two novel mutations and coexistence of the 991C>T and the 1339C>T ...
... in Swedish patients with hereditary coproporphyria. Wiman A, Floderus Y, ... Hereditary coproporphyria (HCP) is an autosomal dominant disorder, resulting ...
http://www.ncbi.nlm.nih.gov/pubmed/12181641
www.ncbi.nlm.nih.gov
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summary
A molecular defect in coproporphyrinogen oxidase gene causing ...
... gene causing harderoporphyria, a variant form of hereditary coproporphyria. ... Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal ...
http://www.ncbi.nlm.nih.gov/pubmed/7757079
www.ncbi.nlm.nih.gov
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Porphyria - OMIM - Genetic disorder catalog - Genetics Home Reference
OMIM: Hereditary Coproporphyria. OMIM: Porphyria Cutanea Tarda and Hepatoerythropoietic Porphyria ... Lister Hill National Center for Biomedical Communications ...
http://ghr.nlm.nih.gov/condition=porphyria/show/OMIM
ghr.nlm.nih.gov
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Ministry Health Care
Hereditary angioedema (Condition) Hereditary coproporphyria (Condition) ... Hereditary sensory and autonomic neuropathy - type III (HSAN III) (Condition) ...
http://ministryhealth.adam.com/content.aspx?productId=26&pid=26&alpha=H
ministryhealth.adam.com
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summary
Cl 13,900 Dihydrochloride(Puy) - NextBio
You must enable JavaScript to run the NextBio application ... ferrochelatase fibroblasts Hereditary coproporphyria IL8RA influenza ...
http://www.nextbio.com/b/home/home.nb?q=Puy
www.nextbio.com
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summary
Characterization and expression of cDNA encoding coproporphyrinogen ...
... coproporphyrinogen oxidase from a patient with hereditary coproporphyria. ... Hereditary coproporphyria (HCP) is an acute hepatic porphyria with autosomal ...
http://www.ncbi.nlm.nih.gov/pubmed/7849704
www.ncbi.nlm.nih.gov
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summary
adam.about.com/encyclopedia/alphaidxh.htm?p=1
Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ... Hereditary sensory and autonomic neuropathy - type III. Hereditary spherocytosis ...
http://adam.about.com/encyclopedia/alphaidxh.htm?p=1
adam.about.com
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summary
Porphyria, Variegate
Important It is possible that the main title of the report Porphyria, Variegate ... it is important to distinguish Varigate Porphyria or hereditary coproporphyria ...
http://www.webmd.com/a-to-z-guides/porphyria-variegate
www.webmd.com
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summary
Human hereditary hepatic porphyrias.
The human hereditary hepatic porphyrias are diseases due to marked deficiencies ... cutanea tarda (PCT), hereditary coproporphyria (HC), and variegate porphyria (VP) ...
http://www.ncbi.nlm.nih.gov/pubmed/12367763
www.ncbi.nlm.nih.gov
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Porphyria, Variegate - Yahoo! Health
Important It is possible that the main title of the report Porphyria, Variegate ... it is important to distinguish Varigate Porphyria or hereditary coproporphyria ...
http://health.yahoo.com/blood-overview/porphyria-variegate/h...
health.yahoo.com
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summary
Delayed diagnosis of porphyria based on manifestations of systemic ...
... who was diagnosed with hereditary coproporphyria after 5 years of follow-up. ... Coproporphyria, Hereditary/diagnosis* Female. Humans. Lupus Erythematosus, ...
http://www.ncbi.nlm.nih.gov/pubmed/17048215
www.ncbi.nlm.nih.gov
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summary
Introduction: Porphyrias: Merck Manual Home Edition
Porphyrias are a group of disorders caused by deficiencies of enzymes involved ... include variegate porphyria, hereditary coproporphyria, and the extremely rare ...
http://www.merck.com/mmhe/print/sec12/ch160/ch160a.html
www.merck.com
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New Descriptors by Tree Subcategory - 2005
Coproporphyria, Hereditary. Gastrointestinal Stromal Tumors. Hepatic Insufficiency ... Coproporphyria, Hereditary. Fetal Nutrition Disorders. Porphyria, Variegate ...
http://www.nlm.nih.gov/mesh/newbysub2005.html
www.nlm.nih.gov
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Encyclopedia - DukeHealth.org
A comprehensive resource for general health information ... Hereditary angioedema (Condition) Hereditary coproporphyria (Condition) ...
http://dukehealthsystem.adam.com/content.aspx?productId=26&pid=26&alpha=H
dukehealthsystem.adam.com
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summary
Loyola University Health System
myLoyola provides you a customized interaction with Loyola University Health System ... Hereditary angioedema (Condition) Hereditary coproporphyria (Condition) ...
http://loyolauniversity.adam.com/content.aspx?productId=26&alpha=H
loyolauniversity.adam.com
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summary
Encyclopedia P-Pz on Yahoo! Health
Health encyclopedia of diseases and conditions covering symptoms, definitions, alternative names, causes, ... Hereditary Coproporphyria. Porphyria, ...
http://health.yahoo.com/ency/p/
health.yahoo.com
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121300
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121300
www.ncbi.nlm.nih.gov
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summary
H
A member of SSM Health Care. Body, Mind, Spirit... We care for the whole person. ... Hereditary angioedema (Condition) Hereditary coproporphyria (Condition) ...
http://ssmhealth.adam.com/content.aspx?productId=26&pid=26&a...
ssmhealth.adam.com
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summary
Localization of the human coproporphyrinogen oxidase gene to chromosome ...
... coproporphyrinogen oxidase is the defective gene in hereditary coproporphyria. This gene was mapped to chromosome band 3q12 using fluorescent in situ ...
http://www.ncbi.nlm.nih.gov/pubmed/7959694
www.ncbi.nlm.nih.gov
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summary
Coproporphyrinogen III oxidase - Wikipedia, the free encyclopedia
Homozygous hereditary coproporphyria caused by an arginine to tryptophane ... Hereditary coproporphyria: exon screening by heteroduplex analysis detects three ...
http://en.wikipedia.org/wiki/Coproporphyrinogen_III_oxidase
en.wikipedia.org
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summary
Wyeth.com | ADAM
Wyeth pharmaceutical company brings health care products, medicines and vaccines ... Hereditary amyloidosis. Hereditary angioedema. Hereditary coproporphyria ...
http://wyeth.adam.com/content.aspx?productId=101&alpha=H
wyeth.adam.com
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HCP - Wikipedia, the free encyclopedia
Hereditary coproporphyria, a deficiency disease. High Card Points, a contract bridge term ... Hexagonal close-packed is an arrangement of spheres into the ...
http://en.wikipedia.org/wiki/HCP
en.wikipedia.org
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Alcohol and porphyrin metabolism.
Alcohol is a porphyrinogenic agent which may cause disturbances in porphyrin ... variegate porphyria and hereditary coproporphyria) are considered to be ...
http://www.ncbi.nlm.nih.gov/pubmed/10787385
www.ncbi.nlm.nih.gov
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The Atkins Diet as a possible trigger for an ICU admission: a case report.
... and diagnosis of hereditary coproporphyria is described, following a ... The frequency of seizures, motor neuropathy and florid visual hallucinations ...
http://www.ncbi.nlm.nih.gov/pubmed/16573483?ordinalpos=11&it...
www.ncbi.nlm.nih.gov
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