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molybdenum cofactor deficiency type B

MeSH: C565373ORPHA: 308393

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

molybdenum cofactor deficiency that has material basis in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C565373

Orphanet Code

ORPHA:308393
molybdenum cofactor deficiency type B
MeSHC565373
OrphanetORPHA:308393
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
molybdenum cofactor deficiency type B | OrphanDrug