Phenotypes for disease #00568 (MOWS (Mowat-Wilson syndrome), OMIM:235730)

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     
0000060569 Mowat-Wilson syndrome (OMIM:235730) - - Isolated (sporadic) - - - - - Daniel Trujillano 00081000
0000338735 Neurodevelopmental delay, Ventricular septal defect, Patent ductus arteriosus, Complex febrile seizure, Microcephaly, Delayed speech and language development, Hypertelorism, Abnormality of the face, Delayed gross motor development - - Isolated (sporadic) 02y - - - - Andreas Laner 00449560
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