has material basis in germline mutation in ADPRS autosomal recessive disease inherited neurodegenerative disorder neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures https://github.com/monarch-initiative/mondo/issues/9666 https://www.malacards.org/card/neurodegeneration_childhood_onset_stress_induced_with_variable_ataxia_and_seizures CONDSIAS DOID:0070352 UMLS:C4748527 OMIM:618170 Orphanet:694922 MEDGEN:1648391 MONDO:0100095 neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures GARD:0026044 An autosomal recessive neurodegenerative disorder with onset in the first years of life following normal early development, with cyclic episodic deterioration in response to stress, such as infection or febrile illness. The severity is highly variable. The cause is mutations in the ADPRHL2 gene. childhood-onset stress-induced neurodegenerative ataxia-seizure syndrome