Metaphyseal cupping

Symptom Information:

Symptom ID: HPO:0003021
Synonyms:
Metaphyseal cupping [OMIM:Metaphyseal cupping]
Metaphyseal cupping (metacarpals and phalanges) [OMIM:Metaphyseal cupping (metacarpals and phalanges)]
Metaphyseal cupping (proximal tibiae and fibulae, distal ulnae) [OMIM:Metaphyseal cupping (proximal tibiae and fibulae, distal ulnae)]
Quality:
Cross references:
OMIM: "Metaphyseal cupping" [OMIM:Metaphyseal cupping]
OMIM: "Metaphyseal cupping (metacarpals and phalanges)" [OMIM:Metaphyseal cupping (metacarpals and phalanges)]
OMIM: "Metaphyseal cupping (proximal tibiae and fibulae, distal ulnae)" [OMIM:Metaphyseal cupping (proximal tibiae and fibulae, distal ulnae)]
Is a (Direct Parents):
HPO         Abnormality of the metaphyses
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)