OBO ID: DOID:0080539
Term Name: PEHO syndrome Search Ontology:
Synonyms:
Definition: A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss. (4)
References:
Ontology: Human Disease   ( DOID:0080539 )
Relationships
is a type of:
OTHER PEHO syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ZNHIT3 PEHO syndrome 260565
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)
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