Create issue ticket

9 Possible Causes for Jaundice - Harderoporphyria

  • Hereditary Coproporphyria

    , [5] characterized by neonatal jaundice, hyperbilirubinemia, hepatosplenomegaly and skin lesions upon exposure to ultraviolet light. [6] HCP is a rare disease, but the exact[en.wikipedia.org] , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] […] symptoms. [2] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[en.wikipedia.org]

  • Erythropoietic Coproporphyria

    , [5] characterized by neonatal jaundice, hyperbilirubinemia, hepatosplenomegaly and skin lesions upon exposure to ultraviolet light. [6] HCP is a rare disease, but the exact[en.wikipedia.org] , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] […] symptoms. [2] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[en.wikipedia.org]

  • Acute Hepatic Porphyria

    , [5] characterized by neonatal jaundice, hyperbilirubinemia, hepatosplenomegaly and skin lesions upon exposure to ultraviolet light. [6] HCP is a rare disease, but the exact[ippn.info] , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] […] symptoms. [2] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[ippn.info]

  • Porphyria

    , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[house.wikia.com]

  • Erythropoietic Porphyria

    , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[house.wikia.com]

  • X-Linked Erythropoietic Protoporphyria

    , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[house.wikia.com]

  • Acute Intermittent Porphyria

    , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[house.wikia.com]

  • Variegate Porphyria

    , characterized by neonatal jaundice, hyperbilirubinemia, enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[house.wikia.com]

  • Erythropoietic Protoporphyria

    , characterized by neonatal jaundice , hyperbilirubinemia , enlargement of the liver and spleen and skin lesions upon exposure to ultraviolet light.[house.wikia.com] Individuals who are homozygous for a specific mutation (K404E) or compound heterozygous with a null allele in CPOX have a more severe erythropoietic porphyria, harderoporphyria[house.wikia.com]

Further symptoms