Phenotypes for disease #00790 (CSS2;MRD14 (Coffin-Siris syndrome, type 2), OMIM:614607)

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     

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Individual ID     
0000295800 Posteriorly rotated ears, Intellectual disability, mild, Facial asymmetry, High palate, Epicanthus, Abnormality of the hand, Wide nose, Delayed CNS myelination - - Isolated (sporadic) 10y - - - - Andreas Laner 00403053
0000302572 growth delay, short stature, generalized hypotonia, abnormality of the nervous system, global developmental delay, delayed speech and language development, seizures, abnormal corpus callosum morphology, abnormal posterior cranial fossa morphology, Dandy-Walker malformation, cerebellum hypoplasia, posterior pituitary dysgenesis, atrial septal defect, pulmonary venous hypertension, abnormal carotid artery morphology, abnormality of the digestive system, feeding difficulties, poor suck, abnormality of the gastrointestinal tract, gastroesophageal reflux, chronic constipation, intestinal obstruction, abnormality of the vertebral column, joint laxity, coarse facial features, low anterior hairline, ptosis, strabismus, depressed nasal bridge, wide nose, anteverted nares, thick nasal alae, broad philtrum, thick vermillon border, delayed eruption of teeth, high palate, prominent eyelashes, thick eyebrow, hypertrichosis, small nail, sparse scalp hair, hepatoblastoma Coffin-Siris syndrome CSS2 Isolated (sporadic) 01y - 00y - - Eugenio Zapata-Aldana 00410468
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