Previous symbols: NTRKR2, BDB, BDB1.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Autosomal Recessive Robinow Syndrome | causative loss of function |
mechanism: Biallelic ROR2 Loss of Function
variant: ROR2 c.1096C>T; p.(Arg366Trp); ROR2 c.1324C>T; p.(Arg442*); ROR2 c.1366dup; p.(Leu456Profs*3); ROR2 c.1970G>A; p.(Arg657His); ROR2 c.2074C>A; p.(Pro692Thr); ROR2 c.2T>G; ROR2 c.323G>A; p.(Arg108Gln); ROR2 c.355C>T; p.(Arg119*) and 3 more
|
| Brachydactyly Type B1 | causative germline gain of function |
mechanism: Truncated ROR2 Receptor with a Specific Mutational Effect
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.