Global Variome shared LOVD

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Phenotype #0000278885 Individual ID 00385102 Associated disease NDD Diagnosis/Initial PHEO syndrome Diagnosis/Definite PCH2E Phenotype details see paper; ..., severe global developmental delay (HP:0001263), profound intellectual disability (HP:0001249), microcephaly (HP:0000252), limb and facila edema (HP:0000969), early-onset epilepsy (HP:0001250), spasticity (HP:0001257), optic atrophy (HP:0001138); abnormal brain morphology (HP:0012443), normal/mild unspecific anomalies early in life followed by cerebellar and cerebral atrophy; no cholestasis (-HP:0001396); failure to thrive (HP:0001508) Inheritance Familial, autosomal recessive Age/Examination 11y (11 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-10-06 16:51:44 +02:00 (CEST) Date last edited 2021-10-07 09:59:10 +02:00 (CEST)

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