Enlarged epiphyses

Symptom Information:

Symptom ID: HPO:0010580
Synonyms:
Large epiphyses [HPO:0010580]
Widened, distorted epiphyses [HPO:0010580]
Enlarged epiphyses [OMIM:Enlarged epiphyses]
Large epiphyses [OMIM:Large epiphyses]
Widened, distorted epiphyses [OMIM:Widened, distorted epiphyses]
Enlarged epiphyses (metatarsals and phalanges) [OMIM:Enlarged epiphyses (metatarsals and phalanges)]
Quality:
Cross references:
OMIM: "Enlarged epiphyses" [OMIM:Enlarged epiphyses]
OMIM: "Large epiphyses" [OMIM:Large epiphyses]
OMIM: "Widened, distorted epiphyses" [OMIM:Widened, distorted epiphyses]
OMIM: "Enlarged epiphyses (metatarsals and phalanges)" [OMIM:Enlarged epiphyses (metatarsals and phalanges)]
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)
                   Enlarged epiphyses(HPO:0010580)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Dent disease type 1 (Orphanet:93622)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Keipert syndrome (Orphanet:2662)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
SHORT syndrome (Orphanet:3163)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
Stickler syndrome type 3 (Orphanet:166100)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
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)
Weissenbacher- Zweymuller syndrome (Orphanet:3450)