Metadata | |
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ID | DOID:0080518 |
Name | Meier-Gorlin syndrome 7 |
Definition | A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC45 gene on chromosome 22q11. https://pubmed.ncbi.nlm.nih.gov/27374770/ |
Xrefs | |
Parent Relationships | |
Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |