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Up to: Congenital nervous system disorder · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Autosomal recessive degenerative and progressive cerebellar ataxia · Partial duplication of the short arm of chromosome 16
Congenital cataracts-facial dysmorphism-neuropathy syndrome
Congenital Cataracts Facial Dysmorphism Neuropathy (CCFDN) syndrome is a complex developmental disorder of autosomal recessive inheritance.
This condition has no sub-types.