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MIM:310465 - N SYNDROME; NSX
Xenbase Genes: pola1
Human Disease Resource: MIM
MONDO:0010686 - manual digit phalanx cartilage element |
Disease Ontology (DO):
DOID:0050769 - N syndrome |
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MONDO:0010686 - manual digit phalanx cartilage element |
DOID:0050769 - N syndrome |