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coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An autosomal recessive syndrome characterized by severe microphthalmia, profound congenital sensorineural hearing loss, lack of pigment in the hair, skin, and eyes, macrocephaly, facial dysmorphism, and osteopetrosis.
Mondo Term and Equivalent IDs
MONDO:0015014:  coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness
UMLS:C4310625: