Alobar holoprosencephaly

Symptom Information:

Symptom ID: HPO:0006988
Synonyms:
Alobar holoprosencephaly [OMIM:Alobar holoprosencephaly]
Alobar holoprosencephaly (rare) [OMIM:Alobar holoprosencephaly (rare)]
Quality:
Cross references:
OMIM: "Alobar holoprosencephaly" [OMIM:Alobar holoprosencephaly]
OMIM: "Alobar holoprosencephaly (rare)" [OMIM:Alobar holoprosencephaly (rare)]
Is a (Direct Parents):
HPO         Holoprosencephaly
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

3q13 microdeletion syndrome (Orphanet:1621)
HOLOPROSENCEPHALY 1 (OMIM:236100)