Phenotype #0000295658

Individual ID 00402907
Associated disease NDD
Diagnosis/Initial neurodevelopmental delay
Diagnosis/Definite -
Phenotype details no perinatal findings; no dysmorphism; no developmental delay; normal behavior; normal growth; motor neuropathy with secondary myopathic involvement; ophthalmology normal; no hearing loss; severe scoliosis, pes cavus, hammer toes; CPKemia
Inheritance Familial, autosomal recessive
Age/Examination 27y (27 years)
Age/Diagnosis -
Age/Onset 15y
Phenotype/Onset -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-02-14 10:40:27 +01:00 (CET)
Date last edited N/A

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