microcephaly Disease Ontology Browser

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Disease Ontology Browser

microcephaly (DOID:10907)
Alliance: disease page
Synonyms: Microcephalus; microencephaly
Alt IDs: ICD10CM:Q02, ICD9CM_2006:742.1, ICD9CM:742.1, MESH:D008831, NCI:C85874, UMLS_CUI:C0025958
Definition: A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants.

Disease References using Mouse Models (9)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Copyright, and Privacy Statement Send questions and comments to User Support.	last database update 01/17/2023 MGI 6.22

Allelic Composition	Genetic Background	Reference	Phenotypes
AspmGt(AJ0069)Wtsi/AspmGt(AJ0069)Wtsi	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	J:164424	View
AspmGt(AA0137)Wtsi/AspmGt(AA0137)Wtsi	involves: 129P2/OlaHsd * C57BL/6JOlaHsd	J:164424	View
Aspmtm1(cre)Mrc/Aspmtm1(cre)Mrc	Not Specified	J:228026	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Cdk5rap2an/Cdk5rap2an	B6.Cg-Cdk5rap2^an	J:160533	View
Cdk5rap2an/Cdk5rap2an Tyrp1B-lt/Tyrp1B-lt	WBB6F1	J:160533	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Mcph1Gt(RRO608)Byg/Mcph1Gt(RRO608)Byg	involves: 129P2/OlaHsd * C57BL/6	J:157993	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Copb2em1Rstot/Copb2em2Rstot	involves: C57BL/6 * C57BL/6J * CD-1 * DBA/2	J:252710	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Kif20bmagoo/Kif20bmagoo	involves: BALB/c * C57BL/6	J:242310	View