Term Name: | rhizomelic chondrodysplasia punctata type 5 |
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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 ) |