ZFYVE26

zinc finger FYVE-type containing 26
OMIM: 612012, ClinGen, DECIPHER

14 panels

Panel Reviews Mode of inheritance Details
14 panels

Green ZFYVE26 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 3.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, MIM# 270700
  • Spastic paraplegia and retinal degeneration
  • Kjellin syndrome
  • Parkinsonism

Green ZFYVE26 in Lysosomal Storage Disorder


Level 2: Metabolic conditions
Version 2.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Disorders of autophagy
  • hereditary spastic paraplegia 15 MONDO:0010044

Green ZFYVE26 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

0 reviews Unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services

Green ZFYVE26 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Genetic Health Queensland
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, MIM# 270700
  • hereditary spastic paraplegia 15, MONDO:0010044

Amber ZFYVE26 in Ataxia - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Royal Melbourne Hospital
  • Expert Review Amber
Phenotypes
  • Autosomal recessive spastic paraplegia 15, 270700

Green ZFYVE26 in Leukodystrophy - paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, MIM# 270700

Green ZFYVE26 in Leukodystrophy - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Royal Melbourne Hospital
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, 270700

Green ZFYVE26 in Hereditary Spastic Paraplegia - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Royal Melbourne Hospital
  • Expert list
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, 270700
  • MONDO:0010044

Green ZFYVE26 in Hereditary Spastic Paraplegia


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, MIM# 270700

Green ZFYVE26 in Hereditary Neuropathy - complex


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Royal Melbourne Hospital
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15 MIM#270700

Green ZFYVE26 in Syndromic Retinopathy


Level 2: Ophthalmological disorders
Version 1.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Royal Melbourne Hospital
  • Expert Review Green
  • Expert Review
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive MIM#270700

Green ZFYVE26 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Mackenzie's Mission
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, 270700 (3)

Green ZFYVE26 in Prepair 1000+


Level 2: Screening
Version 3.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Mackenzie's Mission
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive, 270700 (3)

Green ZFYVE26 in Prepair 500+


Level 2: Screening
Version 3.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Mackenzie's Mission
  • Expert Review Green
Phenotypes
  • Spastic paraplegia 15, autosomal recessive MIM#270700