Rickets
Symptom Information:
Symptom ID: | HPO:0002748 | ||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |