Dysmorphic features

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Dysmorphic features (in some patients) [OMIM:Dysmorphic features (in some patients)]
Quality:
Cross references:
OMIM: "Dysmorphic features" [OMIM:Dysmorphic features]
OMIM: "Dysmorphic features (in some patients)" [OMIM:Dysmorphic features (in some patients)]
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)