This is just here as a test because I lose it
Term information
definition
A chromosome microdeletion syndrome with characteristics of neonatal hypotonia, global developmental delay, normal to accelerated growth, absent to severely delayed speech, and minor dysmorphic features.
Term relations
Subclass of:
- Deletion of part of autosome (disorder)
- Deletion of part of autosome (disorder) and Role group (attribute) some (
Associated morphology (attribute) some Partial monosomy (morphologic abnormality) and
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Long arm of chromosome (cell structure) and
Pathological process (attribute) some Pathological developmental process (qualifier value)) and Role group (attribute) some (
Associated morphology (attribute) some Partial monosomy (morphologic abnormality) and
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Chromosome pair 22 (cell structure) and
Pathological process (attribute) some Pathological developmental process (qualifier value))