Normocephaly

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Normocephaly" [OMIM:Normocephaly]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
Cartilage-hair hypoplasia (Orphanet:175)
Diastrophic dwarfism (Orphanet:628)
Dyschondrosteosis - nephritis (Orphanet:1765)
Ellis Van Creveld syndrome (Orphanet:289)
MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE (OMIM:156230)
Mesomelic dwarfism, Reinhardt-Pfeiffer type (Orphanet:2634)
Parastremmatic dwarfism (Orphanet:2646)
Pseudoachondroplasia (Orphanet:750)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT (OMIM:184100)