Normocephaly
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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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) |