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inherited porphyria

Disease Summary
Associated Targets (23)
Tbio

12

Tchem

7

Tclin

4


GARD Rare
Mondo Description Porphyrias constitute a group of eight hereditary metabolic diseases characterized by intermittent neuro-visceral manifestations, cutaneous lesions or by the combination of both.
Disease Ontology Description An inherited metabolic disorder that involves certain enzymes in the heme bio-synthetic pathway resulting in the overproduction and accumulation of the porphyrins.
Mondo Term and Equivalent IDs
MONDO:0019142:  inherited porphyria
COHD:434908: 
GARD:0010353: 
MESH:D011164: 
NCIT:C97096: 
Orphanet:738: 
SCTID:371628009: 
UMLS:C0032708: