Phenotypes for disease #04112 (CSS9;MRD27 (Coffin-Siris syndrome, type 9 (CSS9, mental retardation, autosomal dominant syndrome, type 27 (MRD27))), OMIM:615866)

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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     
0000060887 intellectual disability, microcephaly, absence seizures; height 89.4 cm (0.4th), weight 12.15 kg (0.4th), OFC 46.5 cm (0.4th); 30m-walk, no speech, poor feeding as neonate, autism, 5th finger clinodactyly, hypoplasia nail 5th toe, oculomotor apraxia Coffin-Siris syndrome - Isolated (sporadic) 12y06m - - - - Alisdair McNeill 00081322
0000060888 microcephaly, developmental delay; height 109.4 cm (9th), weight 18.45 kg (9th), OFC 48.2 cm (0.4th); 30m-walk; 36m-speech; poor feeding as neonate, 5th finger clinodactyly, 2–3 toe syndactyly, hypoplasia nail 5th toe, hypermetropia Coffin-Siris syndrome CSS9 Isolated (sporadic) 11y - - - - Alisdair McNeill 00081323
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