Phenotypes for disease #00877 (3M2 (3M syndrome, type 2 (3M2)), OMIM:612921)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000117210 HP:0007503 (Generalized Ichthyosis); HP:0001264 (spastic diplegia); HP:0001249 (intellectual disability); HP:0000613 (photophobia); HP:0001622 (premature birth, 32 weeks); HP:0001347 (Hyperreflexia) - - Familial, autosomal recessive 03y - - - - Maximilian Weustenfeld 00144443
0000325453 Myopathy - - Unknown - - - - - Marco Savarese 00435256
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