Normal height
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 8 / 7739 | |
Resource: |
All diseases associated with this symptom:
1q21.1 microduplication syndrome | (Orphanet:250994) |
Autosomal dominant osteosclerosis, Worth type | (Orphanet:2790) |
Muenke syndrome | (Orphanet:53271) |
OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIANBONES, BUT WITHOUT FRACTURES | (OMIM:166230) |
STICKLER SYNDROME, TYPE I | (OMIM:108300) |
Stickler syndrome type 2 | (Orphanet:90654) |
TARSAL-CARPAL COALITION SYNDROME | (OMIM:186570) |
THORACOLARYNGOPELVIC DYSPLASIA | (OMIM:187760) |