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

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

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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
0000356991 Coffin-Siris syndrome, CSS6 retrognathia, coarse facial features, a short philtrum, a prominent forehead, low-set and posteriorly rotated ears, a broad nasal tip, downslanting palpebral fissures, and intermittent exotropiaï¼›Pathological diagnosis: Consistent with non-specific cirrhotic pathological changes. Familial, autosomal dominant - 7 - - Guorui Hu 00472182
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