porphyria cutanea tarda

Preferred Label : porphyria cutanea tarda;

MeSH definition : An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.;

Wikipedia link : https://en.wikipedia.org/wiki/Porphyria cutanea tarda;

Details

Origin ID

D017119;

UMLS CUI

C0162566;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- CALCA wt Allele [NCIt concept]
- Familial porphyria cutanea tarda [ICD-11 More detail]
- Percent (property) (qualifier value) [SNOMED CT concept]
- Prevention, Clinical, and Therapeutic Subcommittee [NCIt concept]
- Procalcitonin Measurement [NCIt concept]
- Sporadic porphyria cutanea tarda [ICD-11 More detail]
- UROD wt Allele [NCIt concept]
- prothrombin consumption time, nos [SNOMED Notion]
DO Cross reference
- porphyria cutanea tarda [DO Concept]
Has phenotype(s) (HPO)
- Pseudoscleroderma [HPO term]
Manual NTBT mappings (CISMeF)
- Chronic hepatic porphyria [ORDO Disease]
- Genodermatosis with ocular features [ORDO Disease]
ORDO relation(s)
- Porphyria cutanea tarda [ORDO Disease]
Record concept(s)
- porphyria cutanea tarda [MeSH concept]
Related MeSH Supplementary Concept(s)
- porphyria cutanea tarda, type I [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cutaneous hepatic porphyria [MedDRA LLT]
- Porphyria Cutanea Tarda [NCIt concept]
- Porphyria cutanea tarda [ORDO Disease]
- Porphyria cutanea tarda [ICD-10 Sub-category]
- Porphyria cutanea tarda [OMIM Phenotype]
- Porphyria cutanea tarda [ICD-10 Sub-category (who)]
- Porphyria cutanea tarda [PASCAL descriptor]
- Porphyria cutanea tarda [ICD-11 Sub-sub category]
- Porphyria cutanea tarda [MedDRA LLT]
- Porphyria cutanea tarda (disorder) [SNOMED CT concept]
- porphyria cutanea tarda [DO Concept]
- porphyria cutanea tarda [Disease (Nov.)]
- porphyria cutanea tarda, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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