Entry Topical Term

Number of records used in: 1

001 - CONTROL NUMBER

• control field: 80877

003 - CONTROL NUMBER IDENTIFIER

• control field: OSt

005 - DATE AND TIME OF LATEST TRANSACTION

• control field: 20191028105542.0

008 - FIXED-LENGTH DATA ELEMENTS

• fixed length control field: 900312i| anannbab| |a ana

010 ## - LIBRARY OF CONGRESS CONTROL NUMBER

• LC control number: sh 90001240

035 ## - SYSTEM CONTROL NUMBER

• System control number: 392051
• Canceled/invalid system control number: sh90001240

040 ## - CATALOGING SOURCE

• Original cataloging agency: DLC
• Transcribing agency: DLC
• Modifying agency: DLC

053 ## - LC CLASSIFICATION NUMBER

• Classification number element--single number or beginning number of span: RJ496.A32

150 ## - HEADING--TOPICAL TERM

• Topical term or geographic name entry element: Adrenoleukodystrophy

450 ## - SEE FROM TRACING--TOPICAL TERM

• Topical term or geographic name entry element: ALD (Disease)

450 ## - SEE FROM TRACING--TOPICAL TERM

• Topical term or geographic name entry element: Neonatal adrenoleukodystrophy

450 ## - SEE FROM TRACING--TOPICAL TERM

• Topical term or geographic name entry element: Siemerling-Crentzfeldt disease

550 ## - SEE ALSO FROM TRACING--TOPICAL TERM

• Control subfield: g
• Topical term or geographic name entry element: Nerves, Peripheral
• General subdivision: Diseases

670 ## - SOURCE DATA FOUND

• Source citation: Work cat.: International Workshop on Adrenoleukodystrophy and Peroxisomal Disorders (1989 : Rome, Italy). Adrenoleukodystrophy and other peroxisomal disorders : clinical, biochemical, genetic, and therapeutic aspects : proceedings ... Rome, 10-11 November 1989
• Information found: (ALD)

670 ## - SOURCE DATA FOUND

• Source citation: MESH.

670 ## - SOURCE DATA FOUND

• Source citation: Merck
• Information found: ("... is a rare, sex-linked recessive metabolic disorder that occurs in boys and is characterized by adrenal atrophy, and widespread, diffuse cerebral demyelination")

670 ## - SOURCE DATA FOUND

• Source citation: Merritt's textbk. neurol.:
• Information found: pp. 536-537 ("the basic defect involves the fatty acids gb soxydation system in subcellar organelles, called peroxisomes, which break down very long chain fatty acids (VLCFAs). Consequently these acids accumulate in tissue and plasma")

670 ## - SOURCE DATA FOUND

• Source citation: Dorland's med. dict.

670 ## - SOURCE DATA FOUND

• Source citation: Stedman's med. dict.
• Information found: (Siemerling-Crentzfeldt disease)

670 ## - SOURCE DATA FOUND

• Source citation: Gould med. dict.