Metaphyseal irregularity

Symptom Information:

Symptom ID: HPO:0003025
Synonyms:
Frayed, irregular metaphyses [HPO:0003025]
Frayed, irregular, metaphyses [HPO:0003025]
Irregular metaphyses [HPO:0003025]
Metaphyseal fraying [HPO:0003025]
Metaphyseal irregularities [HPO:0003025]
Frayed, irregular metaphyses [OMIM:Frayed, irregular metaphyses]
Frayed, irregular, metaphyses [OMIM:Frayed, irregular, metaphyses]
Irregular metaphyses [OMIM:Irregular metaphyses]
Metaphyseal irregularities [OMIM:Metaphyseal irregularities]
Metaphyseal irregularity [OMIM:Metaphyseal irregularity]
Irregular metaphyses (childhood) [OMIM:Irregular metaphyses (childhood)]
Metaphyseal irregularities (distal femora, proximal and distal tibiae, distal radii and ulnae) [OMIM:Metaphyseal irregularities (distal femora, proximal and distal tibiae, distal radii and ulnae)]
Quality:
Cross references:
OMIM: "Frayed, irregular metaphyses" [OMIM:Frayed, irregular metaphyses]
OMIM: "Frayed, irregular, metaphyses" [OMIM:Frayed, irregular, metaphyses]
OMIM: "Irregular metaphyses" [OMIM:Irregular metaphyses]
OMIM: "Metaphyseal irregularities" [OMIM:Metaphyseal irregularities]
OMIM: "Metaphyseal irregularity" [OMIM:Metaphyseal irregularity]
OMIM: "Irregular metaphyses (childhood)" [OMIM:Irregular metaphyses (childhood)]
OMIM: "Metaphyseal irregularities (distal femora, proximal and distal tibiae, distal radii and ulnae)" [OMIM:Metaphyseal irregularities (distal femora, proximal and distal tibiae, distal radii and ulnae)]
Is a (Direct Parents):
HPO         Lower-limb metaphyseal irregularity
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)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of the metaphyses(HPO:0000944)
                   Metaphyseal irregularity(HPO:0003025)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the metaphyses(HPO:0000944)
                      Metaphyseal irregularity(HPO:0003025)
MedDRA:
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

Dent disease type 1 (Orphanet:93622)
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE (OMIM:610797)
Free sialic acid storage disease, infantile form (Orphanet:309324)
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)
Jeune syndrome (Orphanet:474)
Lethal Kniest-like dysplasia (Orphanet:2347)
METAPHYSEAL ANADYSPLASIA 2 (OMIM:613073)
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS (OMIM:250460)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Metaphyseal dysostosis - intellectual deficit - conductive deafness (Orphanet:2502)
Mucopolysaccharidosis type 6 (Orphanet:583)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Orofaciodigital syndrome type 2 (Orphanet:2751)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SPONASTRIME dysplasia (Orphanet:93357)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Schneckenbecken dysplasia (Orphanet:3144)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Smith-McCort dysplasia (Orphanet:178355)
Spondylo-megaepiphyseal-metaphyseal dysplasia (Orphanet:228387)
Spondyloepimetaphyseal dysplasia - abnormal dentition (Orphanet:168451)
Spondyloepimetaphyseal dysplasia congenita, Strudwick type (Orphanet:93346)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepimetaphyseal dysplasia, Geneviève type (Orphanet:168454)
Spondyloepimetaphyseal dysplasia, Shohat type (Orphanet:93352)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
Spondylometaphyseal dysplasia, 'corner fracture' type (Orphanet:93315)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
Spondylometaphyseal dysplasia, Kozlowski type (Orphanet:93314)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia type 1 (Orphanet:1860)
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)
X-linked hypophosphatemia (Orphanet:89936)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)