Metaphyseal widening

Symptom Information:

Symptom ID: HPO:0003016
Synonyms:
Wide metaphyses [HPO:0003016]
Widened long bone metaphyses [HPO:0003016]
Widened metaphyses [HPO:0003016]
Metaphyseal widening [OMIM:Metaphyseal widening]
Wide metaphyses [OMIM:Wide metaphyses]
Widened metaphyses [OMIM:Widened metaphyses]
Wide metaphyses (metacarpals and phalanges) [OMIM:Wide metaphyses (metacarpals and phalanges)]
Wide metaphyses (metatarsals and phalanges) [OMIM:Wide metaphyses (metatarsals and phalanges)]
Wide metaphyses (rare) [OMIM:Wide metaphyses (rare)]
Widened metaphyses (elbows and knees) [OMIM:Widened metaphyses (elbows and knees)]
Widened metaphyses (metacarpal and phalanges) [OMIM:Widened metaphyses (metacarpal and phalanges)]
Quality:
Cross references:
OMIM: "Metaphyseal widening" [OMIM:Metaphyseal widening]
OMIM: "Wide metaphyses" [OMIM:Wide metaphyses]
OMIM: "Widened metaphyses" [OMIM:Widened metaphyses]
OMIM: "Wide metaphyses (metacarpals and phalanges)" [OMIM:Wide metaphyses (metacarpals and phalanges)]
OMIM: "Wide metaphyses (metatarsals and phalanges)" [OMIM:Wide metaphyses (metatarsals and phalanges)]
OMIM: "Wide metaphyses (rare)" [OMIM:Wide metaphyses (rare)]
OMIM: "Widened metaphyses (elbows and knees)" [OMIM:Widened metaphyses (elbows and knees)]
OMIM: "Widened metaphyses (metacarpal and phalanges)" [OMIM:Widened metaphyses (metacarpal and phalanges)]
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 widening(HPO:0003016)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of the metaphyses(HPO:0000944)
                   Metaphyseal widening(HPO:0003016)
MedDRA:
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:123000)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cartilage-hair hypoplasia (Orphanet:175)
Craniometaphyseal dysplasia (Orphanet:1522)
DESBUQUOIS DYSPLASIA 1 (OMIM:251450)
DESBUQUOIS DYSPLASIA 2 (OMIM:615777)
Desbuquois syndrome (Orphanet:1425)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
FIBROCHONDROGENESIS 2 (OMIM:614524)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Goldblatt syndrome (Orphanet:166272)
Hallermann-Streiff syndrome (Orphanet:2108)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
METAPHYSEAL ANADYSPLASIA 2 (OMIM:613073)
Menkes disease (Orphanet:565)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Metaphyseal chondrodysplasia, Spahr type (Orphanet:2501)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
Osteoporosis - pseudoglioma (Orphanet:2788)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE (OMIM:611702)
Schwartz-Jampel syndrome (Orphanet:800)
Short-rib thoracic dysplasia 3 with or without polydactyly (OMIM:613091)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Shwachman-Diamond syndrome (Orphanet:811)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
THORACOLARYNGOPELVIC DYSPLASIA (OMIM:187760)
Thoracolaryngopelvic dysplasia (Orphanet:3317)
Torg-Winchester syndrome (Orphanet:3460)