Phenotypes for disease #05234 (CM1 (malformation, Chiari, type I (CM-1)), OMIM:118420)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000078872 - - - Familial, autosomal dominant 08y 08y scaphocephaly, Chiari malformation type I - Patrizia De Marco 00100621
0000078875 hypertelorism, prominent head, epicanthus, clinodactyly, psycho-motor delay - - Familial, autosomal dominant 12y 12y - - Patrizia De Marco 00100647
0000078880 syringomyelia - - Isolated (sporadic) 05y 05y - - Patrizia De Marco 00100655
0000078881 cerebellar lipoma, hydrocephalus - - Isolated (sporadic) 16y 09y - - Patrizia De Marco 00100656
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