Abnormality of the lower limb

Symptom Information:

Symptom ID: HPO:0002814
Synonyms:
Lower limb deformities [HPO:0002814]
Lower limb segmental anomaly [Orphanet:21000]
Lower limb deformities [OMIM:Lower limb deformities]
Lower limb segmental anomalies [Orphanet:21000]
Lower limb deformities (69%) [OMIM:Lower limb deformities (69%)]
Lower limb deformities (childhood-onset) [OMIM:Lower limb deformities (childhood-onset)]
Quality:
Cross references:
Orphanet:21000 "Lower limb segmental anomalies" [Orphanet:21000]
OMIM: "Lower limb deformities" [OMIM:Lower limb deformities]
OMIM: "Lower limb deformities (69%)" [OMIM:Lower limb deformities (69%)]
OMIM: "Lower limb deformities (childhood-onset)" [OMIM:Lower limb deformities (childhood-onset)]
Is a (Direct Parents):
HPO         Abnormality of lower limb bone
HPO         Abnormality of limb bone morphology
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 appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the lower limb(HPO:0002814)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

Adams-Oliver syndrome (Orphanet:974)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Autosomal dominant hypophosphatemic rickets (Orphanet:89937)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
Dent disease type 1 (Orphanet:93622)
Diabetic embryopathy (Orphanet:1926)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Familial multiple nevi flammei (Orphanet:624)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hereditary hypophosphatemic rickets with hypercalciuria (Orphanet:157215)
Ito hypomelanosis (Orphanet:435)
Metaphyseal anadysplasia (Orphanet:1040)
Microphthalmia with limb anomalies (Orphanet:1106)
Moebius syndrome (Orphanet:570)
Nager syndrome (Orphanet:245)
Nail-patella syndrome (Orphanet:2614)
Poland syndrome (Orphanet:2911)
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)