|
MIM:210600 - SECKEL SYNDROME 1; SCKL1
Xenbase Genes: atr
Human Disease Resource: OMIM
MONDO:0008869 - Seckel syndrome 1 |
MONDO:0019342 - Seckel syndrome |
DOID:0070007 - Seckel syndrome 1 |
|
MONDO:0008869 - Seckel syndrome 1 |
MONDO:0019342 - Seckel syndrome |
DOID:0070007 - Seckel syndrome 1 |