Phenotypes for disease #01651 (AI1G (amelogenesis imperfecta, type IG (AI1G, enamelrenal syndrome)), OMIM:204690)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000085610 Amelogenesis imperfecta; Autosomal recessive hypoplastic amelogenesis imperfecta; Gingival hyperplasia; Pulp stones; Prolonged retention of the deciduous teeth; Delayed or failed eruption of permanent teeth; - - Familial, autosomal recessive - - - - - JUNG-WOOK KIM 00107849
0000085611 Amelogenesis imperfecta; Autosomal recessive hypoplastic amelogenesis imperfecta; Gingival hyperplasia; Pulp stones; Prolonged retention of the deciduous teeth; Delayed or failed eruption of permanent teeth; - - Familial, autosomal recessive - - - - - JUNG-WOOK KIM 00107850
0000085612 Amelogenesis imperfecta; Autosomal recessive hypoplastic amelogenesis imperfecta; Gingival hyperplasia; Pulp stones; Prolonged retention of the deciduous teeth; Delayed or failed eruption of permanent teeth; - - Familial, autosomal recessive - - - - - JUNG-WOOK KIM 00107851
0000085613 Amelogenesis imperfecta; Autosomal recessive hypoplastic amelogenesis imperfecta; Gingival hyperplasia; Pulp stones; Prolonged retention of the deciduous teeth; Delayed or failed eruption of permanent teeth; - - Familial, autosomal recessive - - - - - JUNG-WOOK KIM 00107852
0000325419 Amelogenesis imperfecta, Delayed permanent dentition - - Unknown 11y - - - - Gemeinschaftspraxis für Humangenetik Dresden 00435221
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