autosomal recessive spinocerebellar ataxia 19 (Q21124576)

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human disease
  • Lichtenstein-Knorr syndrome
  • autosomal recessive spinocerebellar ataxia type 19
  • Progressive autosomal recessive ataxia-sensorineural hearing loss syndrome
  • SCAR19
  • LICHTENSTEIN-KNORR SYNDROME; LIKNS
  • LIKNS
  • Progressive autosomal recessive ataxia-deafness syndrome
  • Spinocerebellar Ataxia, Autosomal Recessive 19
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Language Label Description Also known as
English
autosomal recessive spinocerebellar ataxia 19
human disease
  • Lichtenstein-Knorr syndrome
  • autosomal recessive spinocerebellar ataxia type 19
  • Progressive autosomal recessive ataxia-sensorineural hearing loss syndrome
  • SCAR19
  • LICHTENSTEIN-KNORR SYNDROME; LIKNS
  • LIKNS
  • Progressive autosomal recessive ataxia-deafness syndrome
  • Spinocerebellar Ataxia, Autosomal Recessive 19

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