WormBase Tree Display for DO_term: DOID:0070293
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DOID:0070293 | Name | primary autosomal recessive microcephaly 2 with or without cortical malformations | |||
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Status | Valid | ||||
Definition | A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the WDR62 gene on chromosome 19q13. | ||||
Synonym | Exact | MCPH2 | |||
Parent | Is_a | DOID:0070296 | |||
DB_info | Database | OMIM | disease | 604317 | |
Attribute_of | Gene_by_orthology | WBGene00019237 |