Neonatal short-limb short stature
Symptom Information:
Symptom ID: | HPO:0008921 | |||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Growth abnormality(HPO:0001507) Abnormality of body height(HPO:0000002) Short stature(HPO:0004322) Disproportionate short stature(HPO:0003498) Disproportionate short-limb short stature(HPO:0008873) Neonatal short-limb short stature(HPO:0008921) Growth delay(HPO:0001510) Short stature(HPO:0004322) Disproportionate short stature(HPO:0003498) Disproportionate short-limb short stature(HPO:0008873) Neonatal short-limb short stature(HPO:0008921) MedDRA: |
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Database Frequency: | 12 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Achondrogenesis type 1B | (Orphanet:93298) |
Achondroplasia | (Orphanet:15) |
Campomelic dysplasia | (Orphanet:140) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Diastrophic dwarfism | (Orphanet:628) |
Dyssegmental dysplasia, Rolland-Desbuquois type | (Orphanet:156731) |
Ellis Van Creveld syndrome | (Orphanet:289) |
MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE | (OMIM:156230) |
Mesomelic dwarfism, Reinhardt-Pfeiffer type | (Orphanet:2634) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |
Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |