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Searched for "Neuronal Ceroid-Lipofuscinoses".

17 results found on Genetics Home Reference.

  • Kufs disease condition summary
    Related classification: Neuronal Ceroid-Lipofuscinoses
    Related genes:
  • juvenile Batten disease condition summary
    Related classification: Neuronal Ceroid-Lipofuscinoses
    Related genes:
  • late-infantile neuronal ceroid lipofuscinosis condition summary
    Related classification: Neuronal Ceroid-Lipofuscinoses
    Related genes:
  • infantile neuronal ceroid lipofuscinosis condition summary
    Related classification: Neuronal Ceroid-Lipofuscinoses
    Related genes:
  • congenital neuronal ceroid lipofuscinosis condition summary
    Related classification: Neuronal Ceroid-Lipofuscinoses
    Related genes:
  • Northern epilepsy condition summary
    Found in link title: Neuronal Ceroid-Lipofuscinoses
    Related genes:
  • CLN6 gene summary
    Official name: ceroid-lipofuscinosis, neuronal 6, late infantile, variant
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • TPP1 gene summary
    Official name: tripeptidyl peptidase I
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • CLN5 gene summary
    Official name: ceroid-lipofuscinosis, neuronal 5
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • MFSD8 gene summary
    Official name: major facilitator superfamily domain containing 8
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • CLN8 gene summary
    Official name: ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • PPT1 gene summary
    Official name: palmitoyl-protein thioesterase 1
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • CLN3 gene summary
    Official name: ceroid-lipofuscinosis, neuronal 3
    Found in link title: Neuronal Ceroid-Lipofuscinoses
  • CTSD gene summary
    Official name: cathepsin D
    Found: ...been found to cause congenital neuronal ceroid lipofuscinosis (NCL). Congenital NCL is characterized...
  • CTSF gene summary
    Official name: cathepsin F
    Found: ...B. This condition is a type of neuronal ceroid lipofuscinosis (NCL) characterized by progressive...
  • DNAJC5 gene summary
    Official name: DnaJ (Hsp40) homolog, subfamily C, member 5
    Found: ...B. This condition is a type of neuronal ceroid lipofuscinosis (NCL) characterized by progressive...
  • KCTD7 gene information
    Official name: potassium channel tetramerization domain containing 7
    Found: ...material, consistent with neuronal ceroid lipofuscinosis. [MIM:611726] The disease is caused...
 
Published: September 29, 2014