Metaphyseal widening
Symptom Information:
Symptom ID: | HPO:0003016 | |||||||||||
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) Abnormality of long bone morphology(HPO:0011314) Abnormality of the metaphyses(HPO:0000944) Metaphyseal widening(HPO:0003016) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) 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) |