Phenotypes for disease #04634 (IMNEPD (multisystem neurologic, endocrine, and pancreatic disease, infantile-onset (IMNEPD)), OMIM:616263)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000337694 Secondary microcephaly, Progressive gait ataxia, Abnormal foot morphology, Intellectual disability, Sensorineural hearing impairment, Neurodevelopmental delay - - Familial, autosomal recessive 09y - - - - Andreas Laner 00448517
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