Dysmorphic features
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
Is a (Whole tree): |
HPO:
MedDRA: |
||
Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
1q41q42 microdeletion syndrome | (Orphanet:250999) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | (Orphanet:254334) |
DPAGT1-CDG | (Orphanet:86309) |
Perrault Syndrome 1 | (OMIM:233400) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
SLC35A2-CDG | (Orphanet:356961) |