Poor spontaneous movements

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Poor spontaneous movements" [OMIM:Poor spontaneous movements]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Mitochondrial trifunctional protein deficiency (Orphanet:746)
Pontocerebellar hypoplasia type 7 (Orphanet:284339)