Ptosis, mild

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Ptosis, mild (less common) [OMIM:Ptosis, mild (less common)]
Quality:
Cross references:
OMIM: "Ptosis, mild" [OMIM:Ptosis, mild]
OMIM: "Ptosis, mild (less common)" [OMIM:Ptosis, mild (less common)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

MYASTHENIC SYNDROME, CONGENITAL, 13 (OMIM:614750)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)