Low-normal intelligence
Symptom Information:
Symptom ID: | OMIM : No Id available | |
Synonyms: |
|
|
Quality: | ||
Cross references: |
|
|
Is a (Direct Parents): |
|
|
Is a (Whole tree): |
HPO:
MedDRA: |
|
Database Frequency: | 3 / 7739 | |
Resource: |
All diseases associated with this symptom:
16p13.3 microduplication syndrome | (Orphanet:96078) |
MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:615414) |
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency | (Orphanet:353284) |