Flat facial profile

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Flat facial profile" [OMIM:Flat facial profile]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Cleft lip/palate - intestinal malrotation - cardiopathy (Orphanet:2001)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Craniofacial-deafness-hand syndrome (Orphanet:1529)
Down syndrome (Orphanet:870)