Severe micromelia

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Severe micromelia" [OMIM:Severe micromelia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 1B (Orphanet:93298)
Atelosteogenesis type II (Orphanet:56304)
Dyssegmental dysplasia - glaucoma (Orphanet:1804)
Kyphomelic dysplasia (Orphanet:1801)
Short rib-polydactyly syndrome, Saldino-Noonan type (Orphanet:93270)