Phenotypes for disease #05883 (CEBALID (CEBALID syndrome (CEBALID)), OMIM:618774)

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

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000274075 - - Abnormality of the head, Microcephaly, Abnormality of the face, Abnormality of the outer ear, Behavioral abnormality, Global developmental delay, Sleep disturbance, Aplasia/Hypoplasia of the cerebrum, Neurodevelopmental delay, Abnormal ear morphology, Decreased head circumference Isolated (sporadic) 03y - - - Andreas Laner 00380223
0000284838 - - Muscular hypotonia, Global developmental delay, Motor delay, Abnormality of the nasal bridge, Wide nasal bridge, Prominent forehead, Abnormal eyelid morphology, Low-set ears, Thin upper lip vermilion, Edema, Edema of the dorsum of hands, Anteverted nares, Abnormality of earlobe Isolated (sporadic) 00y06m - - - Andreas Laner 00391502
0000351562 Epilepsy, Intellectual disability, Hearing loss - - Unknown - - - - Juliana Mazzeu 00466175
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