Phenotypes for disease #00271 (SCKL2 (Seckel syndrome, type 2 (SCKL-2)), OMIM:606744)

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     
0000002849 microphthalmia, micrognathia, microglossia, and small teeth. Bilateral basal ganglia calcification and cerebellar calcification on brain MRI - - Familial, autosomal recessive - - - - - Fowzan Alkuraya 00004046
0000060434 Seckel syndrome type 2 (OMIM:606744) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080865
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