Rickets

Symptom Information:

Symptom ID: HPO:0002748
Synonyms:
Rickets (disorder) [Orphanet:45090]
Rickets [Orphanet:45090]
Rachitis [Orphanet:45090]
Rickets [OMIM:Rickets]
Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets [Orphanet:45090]
Rickets [MedDRA:10039119]
Active rickets [MedDRA:10039119]
Rickets NOS [MedDRA:10039119]
Rickets, active [MedDRA:10039119]
Rickets, late effect [MedDRA:10039119]
No rickets [OMIM:No rickets]
Rickets (childhood-onset) [OMIM:Rickets (childhood-onset)]
Rickets (hypophosphatasia only) [OMIM:Rickets (hypophosphatasia only)]
Rickets (in approximately 33% of patients) [OMIM:Rickets (in approximately 33% of patients)]
Quality:
Cross references:
Orphanet:45090 "Osteoporosis/osteopenia/demineralisation/osteomalacia/rickets" [Orphanet:45090]
OMIM: "Rickets" [OMIM:Rickets]
OMIM: "No rickets" [OMIM:No rickets]
OMIM: "Rickets (childhood-onset)" [OMIM:Rickets (childhood-onset)]
OMIM: "Rickets (hypophosphatasia only)" [OMIM:Rickets (hypophosphatasia only)]
OMIM: "Rickets (in approximately 33% of patients)" [OMIM:Rickets (in approximately 33% of patients)]
UMLS:C0035579 "Rickets" [HPO:0002748]
UMLS:C0035579 "Rickets" [Orphanet:45090]
UMLS:C0242491 "Rachitis" [Orphanet:45090]
Is a (Direct Parents):
Orphanet Osteopenia
Orphanet Abnormality of the skeletal system
MedDRA Metabolic bone disorders
HPO         Reduced bone mineral density
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)
                      Rickets(HPO:0002748)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Bone disorders (excl congenital and fractures)(MedDRA:10005959)
       Metabolic bone disorders(MedDRA:10027425)
          Rickets(HPO:0002748)
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

Adult hypophosphatasia (Orphanet:247676)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Autosomal recessive hypophosphatemic rickets (Orphanet:289176)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE (OMIM:219900)
Childhood-onset hypophosphatasia (Orphanet:247667)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Cystinosis (Orphanet:213)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
Distal renal tubular acidosis with anemia (Orphanet:93610)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
FANCONI RENOTUBULAR SYNDROME 3 (OMIM:615605)
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG (OMIM:616026)
Familial hypercholanemia (Orphanet:238475)
Fanconi renotubular syndrome 1 (OMIM:134600)
HYPOPHOSPHATEMIC BONE DISEASE (OMIM:146350)
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM (OMIM:612089)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hemochromatosis type 2 (Orphanet:79230)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Hypocalcemic vitamin D-dependent rickets (Orphanet:289157)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
Infantile hypophosphatasia (Orphanet:247651)
Menkes disease (Orphanet:565)
Oculocerebrorenal syndrome (Orphanet:534)
Odontohypophosphatasia (Orphanet:247685)
Primary Fanconi syndrome (Orphanet:3337)
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Orphanet:3390)
RENAL TUBULAR ACIDOSIS III (OMIM:267200)
Tyrosinemia type 1 (Orphanet:882)
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)
Werner syndrome (Orphanet:902)
Wilson disease (Orphanet:905)
Wolcott-Rallison syndrome (Orphanet:1667)
[DEL] RENAL TUBULAR ACIDOSIS, PROXIMAL (OMIM:179830)