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Entry Name Description Category Pathway Gene
H02349 Odontochondrodysplasia
Goldblatt syndrome
Odontochondrodysplasia (ODCD), also known as Goldblatt syndrome, is a genetic disorder of skeletal and dental development. Clinical findings are short stature, narrow chest, mesomelic limb shortening, ... Congenital malformation (ODCD1) TRIP11 [HSA:9321] [KO:K23368]
(ODCD2) MIA3 [HSA:375056] [KO:K23704]
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