Disease #05348 (MIMIS (microcephaly-micromelia syndrome (MIMIS)), OMIM:251230)

Official abbreviation MIMIS
Name microcephaly-micromelia syndrome (MIMIS)
OMIM ID 251230
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene DONSON
Associated tissues -
Disease features -
Remarks autosomal recessive
Date created 2017-11-17 14:47:27 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00133271 - - 2 generation family, 2 affecteds (2F), 4 unaffecteds (3M, 1F) F no Germany European - - - - MIMIS microcephaly radial aplasia - DONSON 2 2 Martin Atta Mensah
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.