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Peroxisome biogenesis disorder 1B

MONDO:0011101

Also known as: peroxisome biogenesis disorder 1B, peroxisome biogenesis disorder 1B (NALD/IRD), peroxisome biogenesis disorder type 1B, PBD1B, Refsum disease, infantile, adrenoleukodystrophy, autosomal neonatal, infantile phytanic acid storage disease, peroxisome biogenesis disorder (NALD/Ird)

9 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Metabolic disease (233) Nervous system disorder (231) Hereditary disease (176) Neurodegenerative disease (171) Peripheral nervous system disorder (114) Central nervous system disorder (107) Neuromuscular disease (106) Peripheral neuropathy (91) Inborn errors of metabolism (45)

Trials to join now! 5 Not yet finished but already full! 1 Completed 2 Terminated 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC