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MIM:617306 - COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD
Xenbase Genes: mitf
Human Disease Resource: MIM
MONDO:0015014 - coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness |
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MONDO:0015014 - coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness |