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MIM:613820 - NEPHRONOPHTHISIS 12; NPHP12
Xenbase Genes: ttc21b
Human Disease Resource: MIM
MONDO:0013442 - nephronophthisis 12 |
MONDO:0019005 - nephronophthisis |
DOID:0111119 - nephronophthisis 12 |
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MONDO:0013442 - nephronophthisis 12 |
MONDO:0019005 - nephronophthisis |
DOID:0111119 - nephronophthisis 12 |