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searching for Hanhart syndrome 3 found (13 total)

Tyrosine aminotransferase (965 words) [view diff] exact match in snippet view article find links to article

in hepatic tyrosine aminotransferase. Tyrosinemia type II (Richner-Hanhart syndrome, RHS) is a disease of autosomal recessive inheritance characterized

Howel–Evans syndrome (1,558 words) [view diff] exact match in snippet view article find links to article

Papillon–Lefèvre syndrome Punctate porokeratotic keratoderma Richner–Hanhart syndrome Schöpf–Schulz–Passarge syndrome Unna Thost disease Vohwinkel syndrome

List of skin conditions (17,965 words) [view diff] exact match in snippet view article find links to article

and soles) Tyrosinemia type II (oculocutaneous tyrosinemia, Richner–Hanhart syndrome) Vohwinkel syndrome (keratoderma hereditaria mutilans, keratoma hereditaria