| Identifier type | ID | Preferred name | Synonyms/notes | Evidence/source |
|---|---|---|---|---|
| OMIM | 606854 | Bilateral frontoparietal polymicrogyria | Common abbreviation: BFPP; classic Mendelian cortical malformation linked to ADGRG1/GPR56 | Piao et al. 2005 (pqac-00000011) |
| MONDO | MONDO_0000087 | polymicrogyria | Broader parent disease term used in OpenTargets disease-target association for ADGRG1 | OpenTargets association (pqac-00000000) |
| MONDO | MONDO_0017091 | bilateral polymicrogyria | Broader bilateral PMG term associated with ADGRG1 in OpenTargets | OpenTargets association (pqac-00000000) |
| OpenTargets target | ENSG00000205336 | ADGRG1 | Approved symbol ADGRG1; former symbol/name GPR56; disease-target evidence links ADGRG1 to polymicrogyria/bilateral polymicrogyria | OpenTargets association (pqac-00000000) |
| Other (gene nomenclature) | — | ADGRG1-related polymicrogyria syndrome | Also described as GPR56-related polymicrogyria; ADGRG1 formerly known as GPR56 | Khatib et al. 2024 (pqac-00000009, pqac-00000015) |
| Other (cytogenetic locus) | 16q12.2-21 | BFPP locus / ADGRG1-linked region | Historical linked interval for autosomal recessive BFPP before/alongside gene definition | Jansen & Andermann 2005 (pqac-00000007); Piao et al. 2005 (pqac-00000008) |
| Other (gene chromosomal location) | 16q21 | ADGRG1 | Gene location reported in recent family report; complements earlier BFPP linkage interval 16q12.2-21 | Khatib et al. 2024 (pqac-00000009) |


*Table: This table summarizes the key nomenclature and identifier anchors for ADGRG1-related bilateral frontoparietal polymicrogyria, including OMIM and MONDO mappings plus gene naming and chromosomal locus information. It is useful for harmonizing disease knowledge base entries across clinical and genomic resources.*