1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070292 | primary autosomal recessive microcephaly 9 | A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |