Irregular epiphyses

Symptom Information:

Symptom ID: HPO:0010582
Synonyms:
Irregular epiphyses [OMIM:Irregular epiphyses]
Irregular epiphyses (childhood) [OMIM:Irregular epiphyses (childhood)]
Irregular epiphyses (knee) [OMIM:Irregular epiphyses (knee)]
Quality:
Cross references:
OMIM: "Irregular epiphyses" [OMIM:Irregular epiphyses]
OMIM: "Irregular epiphyses (childhood)" [OMIM:Irregular epiphyses (childhood)]
OMIM: "Irregular epiphyses (knee)" [OMIM:Irregular epiphyses (knee)]
Is a (Direct Parents):
HPO         Abnormality of epiphysis morphology
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 epiphysis morphology(HPO:0005930)
                   Irregular epiphyses(HPO:0010582)
MedDRA:
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Diastrophic dwarfism (Orphanet:628)
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 (OMIM:600969)
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 (OMIM:614135)
Goldblatt syndrome (Orphanet:166272)
Jeune syndrome (Orphanet:474)
Lowry-Wood syndrome (Orphanet:1824)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Multiple epiphyseal dysplasia due to collagen 9 anomaly (Orphanet:166002)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Pseudoachondroplasia (Orphanet:750)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Smith-McCort dysplasia (Orphanet:178355)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepimetaphyseal dysplasia, Geneviève type (Orphanet:168454)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)