Ten percent of cases are secondary to submicroscopic deletions of 16p13.3 detectable by FISH

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Ten percent of cases are secondary to submicroscopic deletions of 16p13.3 detectable by FISH" [OMIM:Ten percent of cases are secondary to submicroscopic deletions of 16p13.3 detectable by FISH]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)