Osteomalacia

Symptom Information:

Symptom ID: HPO:0002749
Synonyms:
Osteomalacia (disorder) [Orphanet:45090]
Osteomalacia [Orphanet:45090]
Osteomalacia [OMIM:Osteomalacia]
Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets [Orphanet:45090]
Osteomalacia [MedDRA:10031250]
Adult rickets [MedDRA:10031250]
Osteomalacia, unspecified [MedDRA:10031250]
Osteomalacia (hypophosphatasia only) [OMIM:Osteomalacia (hypophosphatasia only)]
Quality:
Cross references:
Orphanet:45090 "Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets" [Orphanet:45090]
OMIM: "Osteomalacia" [OMIM:Osteomalacia]
OMIM: "Osteomalacia (hypophosphatasia only)" [OMIM:Osteomalacia (hypophosphatasia only)]
UMLS:C0029442 "Osteomalacia" [HPO:0002749]
UMLS:C0029442 "Osteomalacia" [Orphanet:45090]
Is a (Direct Parents):
Orphanet Osteopenia
Orphanet Abnormality of the skeletal system
HPO         Reduced bone mineral density
MedDRA Metabolic bone disorders
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)
             Abnormal bone structure(HPO:0003330)
                Abnormality of bone mineral density(HPO:0004348)
                   Reduced bone mineral density(HPO:0004349)
                      Osteomalacia(HPO:0002749)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Metabolic bone disorders(MedDRA:10027425)
          Osteomalacia(HPO:0002749)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

AXIAL OSTEOMALACIA (OMIM:109130)
Adult hypophosphatasia (Orphanet:247676)
Autosomal dominant distal renal tubular acidosis (Orphanet:93608)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cystinosis (Orphanet:213)
Dent disease type 1 (Orphanet:93622)
Distal renal tubular acidosis (Orphanet:18)
Fanconi renotubular syndrome 1 (OMIM:134600)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
HYPOPHOSPHATEMIC BONE DISEASE (OMIM:146350)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hemochromatosis type 2 (Orphanet:79230)
Menkes disease (Orphanet:565)
OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION (OMIM:259660)
Oculocerebrorenal syndrome (Orphanet:534)
Odontohypophosphatasia (Orphanet:247685)
Primary Fanconi syndrome (Orphanet:3337)
RENAL TUBULAR ACIDOSIS III (OMIM:267200)
Werner syndrome (Orphanet:902)
Wilson disease (Orphanet:905)
Wolcott-Rallison syndrome (Orphanet:1667)
X-linked hypophosphatemia (Orphanet:89936)