Stereotypic movements

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Stereotypic movements" [OMIM:Stereotypic movements]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Adenylosuccinate lyase deficiency (Orphanet:46)
Kleefstra syndrome (Orphanet:261494)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)