Delayed epiphyseal ossification

Symptom Information:

Symptom ID: HPO:0002663
Synonyms:
Delayed epiphyseal maturation [HPO:0002663]
Delayed opacification of the epiphyses [HPO:0002663]
Detailed epiphyseal ossification [HPO:0002663]
Epiphyseal ossification delay [HPO:0002663]
Delayed epiphyseal maturation [OMIM:Delayed epiphyseal maturation]
Delayed epiphyseal ossification [OMIM:Delayed epiphyseal ossification]
Delayed opacification of the epiphyses [OMIM:Delayed opacification of the epiphyses]
Detailed epiphyseal ossification [OMIM:Detailed epiphyseal ossification]
Epiphyseal ossification delay [OMIM:Epiphyseal ossification delay]
Delayed epiphyseal ossification (early) [OMIM:Delayed epiphyseal ossification (early)]
Quality:
Cross references:
OMIM: "Delayed epiphyseal maturation" [OMIM:Delayed epiphyseal maturation]
OMIM: "Delayed epiphyseal ossification" [OMIM:Delayed epiphyseal ossification]
OMIM: "Delayed opacification of the epiphyses" [OMIM:Delayed opacification of the epiphyses]
OMIM: "Detailed epiphyseal ossification" [OMIM:Detailed epiphyseal ossification]
OMIM: "Epiphyseal ossification delay" [OMIM:Epiphyseal ossification delay]
OMIM: "Delayed epiphyseal ossification (early)" [OMIM:Delayed epiphyseal ossification (early)]
Is a (Direct Parents):
HPO         Abnormality of epiphysis morphology
HPO         Abnormal epiphyseal ossification
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)
                   Delayed epiphyseal ossification(HPO:0002663)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal epiphyseal ossification(HPO:0010656)
                      Delayed epiphyseal ossification(HPO:0002663)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Dent disease type 1 (Orphanet:93622)
Dyssegmental dysplasia - glaucoma (Orphanet:1804)
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 (OMIM:600969)
Eiken syndrome (Orphanet:79106)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Kniest dysplasia (Orphanet:485)
Multiple epiphyseal dysplasia type 1 (Orphanet:93308)
Pseudoachondroplasia (Orphanet:750)
SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION (OMIM:182255)
Short stature, Brussels type (Orphanet:2867)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A (OMIM:264700)
VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B (OMIM:600081)
VITAMIN D-DEPENDENT RICKETS, TYPE 2A (OMIM:277440)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)