Metaphyseal cupping
Symptom Information:
Symptom ID: | HPO:0003021 | |||
Synonyms: |
|
|||
Quality: | ||||
Cross references: |
|
|||
Is a (Direct Parents): |
|
|||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the metaphyses(HPO:0000944) Metaphyseal cupping(HPO:0003021) Abnormality of long bone morphology(HPO:0011314) Abnormality of the metaphyses(HPO:0000944) Metaphyseal cupping(HPO:0003021) MedDRA: |
|||
Database Frequency: | 16 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Cartilage-hair hypoplasia | (Orphanet:175) |
Goldblatt syndrome | (Orphanet:166272) |
Greenberg dysplasia | (Orphanet:1426) |
Infantile hypophosphatasia | (Orphanet:247651) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Metaphyseal anadysplasia | (Orphanet:1040) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
Metaphyseal dysostosis - intellectual deficit - conductive deafness | (Orphanet:2502) |
Opsismodysplasia | (Orphanet:2746) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE | (OMIM:613320) |
Spondyloepimetaphyseal dysplasia, Bieganski type | (Orphanet:168448) |
Spondyloepimetaphyseal dysplasia, Missouri type | (Orphanet:93356) |
Spondylometaphyseal dysplasia - cone-rod dystrophy | (Orphanet:85167) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |