Hypophosphatemic rickets

Symptom Information:

Symptom ID: HPO:0004912
Synonyms:
Hypophosphatemic rickets [OMIM:Hypophosphatemic rickets]
Hypophosphatemic rickets (in some patients) [OMIM:Hypophosphatemic rickets (in some patients)]
Quality:
Cross references:
OMIM: "Hypophosphatemic rickets" [OMIM:Hypophosphatemic rickets]
OMIM: "Hypophosphatemic rickets (in some patients)" [OMIM:Hypophosphatemic rickets (in some patients)]
Is a (Direct Parents):
HPO         Rickets
HPO         Hypophosphatemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of ion homeostasis(HPO:0003111)
             Abnormality of phosphate homeostasis(HPO:0100529)
                Hypophosphatemia(HPO:0002148)
                   Hypophosphatemic rickets(HPO:0004912)
       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)
                         Hypophosphatemic rickets(HPO:0004912)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 (OMIM:614473)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Autosomal recessive hypophosphatemic rickets (Orphanet:289176)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Generalized arterial calcification of infancy (Orphanet:51608)
HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM (OMIM:612089)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Hypophosphatemic rickets, autosomal recessive, 2 (OMIM:613312)
Linear nevus sebaceus syndrome (Orphanet:2612)
Tyrosinemia type 1 (Orphanet:882)
X-linked hypophosphatemia (Orphanet:89936)