Global developmental delay, profound

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Global developmental delay, profound" [OMIM:Global developmental delay, profound]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B (OMIM:614678)