Phenotypes associated with the disease cerebral sclerosis similar to Pelizaeus-Merzbacher disease (OMIM:213900):
- Abnormality of the nervous system (HP:0000707): An abnormality of the nervous system. Evidence: IEA. (OMIM:213900)
- Abnormality of metabolism/homeostasis (HP:0001939). Evidence: IEA. (OMIM:213900)
- Autosomal recessive inheritance (HP:0000007): A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). Evidence: IEA. (OMIM:213900)