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Hereditary Neuropathy v2.0 PPOX Gene migrated from ENSG00000143224 to ENSG00000143224 (gene set migration)
Hereditary Neuropathy v1.3 PPOX Zornitza Stark Phenotypes for gene: PPOX were changed from Porphyria variegata, MIM# 176200 to Porphyria variegata, MIM# 176200; Variegate porphyria, childhood-onset, MIM# 620483
Hereditary Neuropathy v1.2 PPOX Zornitza Stark Publications for gene: PPOX were set to
Hereditary Neuropathy v1.1 PPOX Zornitza Stark Mode of inheritance for gene: PPOX was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary Neuropathy v1.0 PPOX Zornitza Stark edited their review of gene: PPOX: Added comment: Bi-allelic variants cause childhood onset disease.; Changed publications: 9811936, 11286631, 33159949; Changed phenotypes: Porphyria variegata, MIM# 176200, Variegate porphyria, childhood-onset, MIM# 620483; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Hereditary Neuropathy v0.43 PPOX Zornitza Stark Marked gene: PPOX as ready
Hereditary Neuropathy v0.43 PPOX Zornitza Stark Gene: ppox has been classified as Green List (High Evidence).
Hereditary Neuropathy v0.43 PPOX Zornitza Stark Classified gene: PPOX as Green List (high evidence)
Hereditary Neuropathy v0.43 PPOX Zornitza Stark Gene: ppox has been classified as Green List (High Evidence).
Hereditary Neuropathy v0.42 PPOX Zornitza Stark gene: PPOX was added
gene: PPOX was added to Hereditary Neuropathy - complex. Sources: NHS GMS
Mode of inheritance for gene: PPOX was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: PPOX were set to Porphyria variegata, MIM# 176200
Review for gene: PPOX was set to GREEN
Added comment: Neuropathy is part of the phenotype.
Sources: NHS GMS