Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Tibial aplasia-ectrodactyly syndrome
Chromosome 17P13.3, telomeric, duplication syndrome
rare
Identifiers
MONDO:0012944
OMIM:612576
Part of
Non-syndromic limb reduction defect
Tibial aplasia-ectrodactyly syndrome
Projects
Sign in to start a project
No projects yet.