Term Name: rhizomelic chondrodysplasia punctata type 1
Synonyms: PBD9, Peroxisome Biogenesis Disorder 9, RCDP1
Definition: A rhizomelic chondrodysplasia punctata that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the PEX7 gene on chromosome 6q23.3.
Ontology: Human Disease [DOID:0110851]   ( DOID:0110851 )

Relationships
is a type of: rhizomelic chondrodysplasia punctata