Term Name: rhizomelic chondrodysplasia punctata type 3
Synonyms: AGPS deficiency, Alkyldihydroxyacetonephosphate Synthase Deficiency, Alkylglycerone-Phosphate Synthase Deficiency, RCDP3
Definition: A rhizomelic chondrodysplasia punctata that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the AGPS gene on chromosome 2q31.2.
Ontology: Human Disease [DOID:0110853]   ( DOID:0110853 )

Relationships
is a type of: rhizomelic chondrodysplasia punctata