Phenotypes for disease #05387 (CSS6 (Coffin-Siris syndrome, type 6 (CSS6)), OMIM:617808)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000272312 - - Abnormality of body height, Abnormality of the face, Downslanted palpebral fissures, Global developmental delay, Growth delay, Abnormal foot morphology, Pes cavus, Abnormal facial shape, Curly hair, Short stature, Abnormality of hair texture, Abnormality of higher mental function, Thyrotoxicosis with diffuse goiter, Neurodevelopmental delay, Cognitive impairment, Graves disease, Slanting of the palpebral fissure Isolated (sporadic) 12y - - - Andreas Laner 00377148
0000312164 - - Intellectual disability, mild, Lateral ventricular asymmetry, Impaired social interactions Isolated (sporadic) 06y - - - Andreas Laner 00420924
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