Normal development

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Normal development (in 2 of 6 patients) [OMIM:Normal development (in 2 of 6 patients)]
Quality:
Cross references:
OMIM: "Normal development" [OMIM:Normal development]
OMIM: "Normal development (in 2 of 6 patients)" [OMIM:Normal development (in 2 of 6 patients)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Beta-ureidopropionase deficiency (Orphanet:65287)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Craniofacial dyssynostosis (Orphanet:1516)
Isolated congenital hypoglossia/aglossia (Orphanet:141152)