The association of amelogenesis imperfecta and a microscopically typical hair dysplasia has been found in several members of a family in two generations. Transmission is X-linked.
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ADULT syndrome
MONDO:0007072
autosomal dominant palmoplantar keratoderma and congenital alopecia
MONDO:0007083
ameloonychohypohidrotic syndrome
MONDO:0007095
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
MONDO:0007124
anonychia with flexural pigmentation
MONDO:0007131
Böök syndrome
MONDO:0007207