ALAGILLE SYNDROME (PATHOLOGY)
  • BT
    DYSPLASIAS + DYSTROPHIES (PATHOLOGY)
  • BT
    HEREDITARY DISEASES, GENETIC DISEASES (MEDICINE)
  • UDC
    616-056.7.000.616-007.17
  • Descriptor GER
    ALAGILLE-SYNDROM (PATHOLOGIE)
  • Descriptor ENG
    ALAGILLE SYNDROME (PATHOLOGY)
  • Descriptor FRE
    SYNDROME D'ALAGILLE (PATHOLOGIE)
  • Variant GER
    SYNDROME/ALAGILLE-SYNDROM (PATHOLOGIE)
  • Variant GER
    ARTERIOHEPATISCHE DYSPLASIE (PATHOLOGIE)
  • Variant GER
    DYSPLASIEN/ARTERIOHEPATISCHE DYSPLASIE (PATHOLOGIE)
  • Variant ENG
    SYNDROMES/ALAGILLE SYNDROME (PATHOLOGY)
  • Variant ENG
    ARTERIOHEPATIC DYSPLASIA (PATHOLOGY)
  • Variant ENG
    DYSPLASIAS/ARTERIOHEPATIC DYSPLASIA (PATHOLOGY)
  • Variant FRE
    ALAGILLE/SYNDROME D'ALAGILLE (PATHOLOGIE)
  • Variant FRE
    DYSPLASIE ARTÉRIO-HÉPATQUE (PATHOLOGIE)
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Last data import from Alma: 1 January 2025