Coxa valga
Symptom Information:
Symptom ID: | HPO:0002673 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
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) Abnormality of the femur(HPO:0002823) Abnormality of the femoral neck or head region(HPO:0003366) Abnormality of the femoral neck(HPO:0003367) Coxa valga(HPO:0002673) MedDRA: |
||||||
Database Frequency: | 57 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES | (OMIM:109120) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
CARPENTER SYNDROME 1 | (OMIM:201000) |
CEREBROOCULOFACIOSKELETAL SYNDROME 1 | (OMIM:214150) |
COFFIN-SIRIS SYNDROME | (OMIM:135900) |
COFS syndrome | (Orphanet:1466) |
CRANIOMETADIAPHYSEAL DYSPLASIA | (OMIM:269300) |
Carpenter syndrome | (Orphanet:65759) |
Coffin-Lowry syndrome | (Orphanet:192) |
Coffin-Siris syndrome | (Orphanet:1465) |
Craniometadiaphyseal dysplasia, wormian bone type | (Orphanet:85184) |
DESBUQUOIS DYSPLASIA 1 | (OMIM:251450) |
DESBUQUOIS DYSPLASIA 2 | (OMIM:615777) |
Desbuquois syndrome | (Orphanet:1425) |
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 | (OMIM:130070) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Familial clubfoot due to 17q23.1q23.2 microduplication | (Orphanet:238578) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Fucosidosis | (Orphanet:349) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
GM1 gangliosidosis type 2 | (Orphanet:79256) |
Geleophysic dysplasia | (Orphanet:2623) |
Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
Holoprosencephaly - craniosynostosis | (Orphanet:2163) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
MGAT2-CDG | (Orphanet:79329) |
Macular coloboma - cleft palate - hallux valgus | (Orphanet:91494) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
Marshall syndrome | (Orphanet:560) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Multiple epiphyseal dysplasia, Beighton type | (Orphanet:166011) |
Occipital horn syndrome | (Orphanet:198) |
Ophthalmomandibulomelic dysplasia | (Orphanet:2741) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Spondyloepimetaphyseal dysplasia with joint laxity | (Orphanet:93359) |
Spondyloepiphyseal dysplasia tarda, Kohn type | (Orphanet:163665) |
Spondylometaphyseal dysplasia, A4 type | (Orphanet:168555) |
Steinert myotonic dystrophy | (Orphanet:273) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
Weaver syndrome | (Orphanet:3447) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
X-linked spondyloepimetaphyseal dysplasia | (Orphanet:93349) |