rare genetic developmental defect during embryogenesis (Q16261): Difference between revisions

Revision as of 20:31, 21 December 2023

human disease

Language	Label	Description	Also known as
English	rare genetic developmental defect during embryogenesis	human disease

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0 references

Revision as of 20:31, 21 December 2023 Fire (talk \| contribs) Bureaucrats, Interface administrators, Administrators 144,819 edits ‎Created claim: instance of (P2): class of disease (Q5294) ← Older edit	Revision as of 20:31, 21 December 2023 Fire (talk \| contribs) Bureaucrats, Interface administrators, Administrators 144,819 edits ‎Created claim: subclass of (P1): rare genetic disease (Q15546) Newer edit →
	Property / subclass of
		rare genetic disease
	Property / subclass of: rare genetic disease / rank
		Normal rank