Term Name: rhizomelic chondrodysplasia punctata type 5
Synonyms: RCDP5
Definition: A rhizomelic chondrodysplasia punctata that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the PEX5 gene on chromosome 12p13.31.
Ontology: Human Disease [DOID:0110854]   ( DOID:0110854 )

Relationships
is a type of: rhizomelic chondrodysplasia punctata