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Disease
Symptom
Infancy onset short-trunk short stature
Symptom Information:
Symptom ID:
HPO:0011406
Synonyms:
Short-trunk dwarfism, identifiable in infancy [HPO:0011406]
Short-trunk dwarfism, identifiable in infancy [OMIM:Short-trunk dwarfism, identifiable in infancy]
Quality:
Cross references:
OMIM: "Short-trunk dwarfism, identifiable in infancy" [OMIM:Short-trunk dwarfism, identifiable in infancy]
Is a (Direct Parents):
HPO
Disproportionate short-trunk short stature
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-trunk short stature(HPO:0003521)
Infancy onset short-trunk short stature(HPO:0011406)
Growth delay(HPO:0001510)
Short stature(HPO:0004322)
Disproportionate short stature(HPO:0003498)
Disproportionate short-trunk short stature(HPO:0003521)
Infancy onset short-trunk short stature(HPO:0011406)
Abnormality of the skeletal system(HPO:0000924)
Abnormality of skeletal morphology(HPO:0011842)
Abnormal axial skeleton morphology(HPO:0009121)
Disproportionate short-trunk short stature(HPO:0003521)
Infancy onset short-trunk short stature(HPO:0011406)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Roifman syndrome
(Orphanet:353298)