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MIM:606744 - SECKEL SYNDROME 2; SCKL2
Xenbase Genes: rbbp8
Human Disease Resource: OMIM
MONDO:0011715 - Seckel syndrome 2 |
MONDO:0019342 - Seckel syndrome |
DOID:0070013 - Seckel syndrome 2 |
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MONDO:0011715 - Seckel syndrome 2 |
MONDO:0019342 - Seckel syndrome |
DOID:0070013 - Seckel syndrome 2 |