[…] recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity varus Club foot Pigeon toe valgus Flat feet Pes cavus Rocker bottom foot Hammer toe Either / both fingers and toes Polydactyly / Syndactyly Webbed toes Arachnodactyly [en.wikipedia.org]

[…] recurvatum Discoid meniscus Congenital patellar dislocation Congenital knee dislocation foot deformity : varus Club foot Pigeon toe valgus Flat feet Pes cavus Rocker bottom foot Hammer toe Either / both fingers and toes Polydactyly / Syndactyly webbed toes Arachnodactyly [ipfs.io]

Achard syndrome (OMIM 100700), a disorder of uncertain origin resembling Marfan syndrome, is characterized by small mandible, arachnodactyly, joint laxity limited to the hands and feet, clubfoot, and bilateral coxa valga (Achard 1902). [rrnursingschool.biz]

[…] joints Arthrogryposis Larsen syndrome RAPADILINO syndrome Axial Skull and face Craniosynostosis Scaphocephaly Oxycephaly Trigonocephaly Craniofacial dysostosis Crouzon syndrome Hypertelorism Hallermann–Streiff syndrome Treacher Collins syndrome other Macrocephaly [en.wikipedia.org]

Arthrogryposis Larsen syndrome Rapadilino syndrome Axial Skull and face Craniosynostosis : Scaphocephaly Oxycephaly Trigonocephaly Craniofacial dysostosis : Crouzon syndrome Hypertelorism Hallermann–Streiff syndrome Treacher Collins syndrome other: Macrocephaly [ipfs.io]

Sprengel's deformity, Wallis Zieff Goldblatt syndrome) knee (Genu valgum, Genu varum) other Arthrogryposis Skull and facial bones Carpenter syndrome - Craniodiaphyseal dysplasia - Craniosynostosis (Scaphocephaly) - Crouzon syndrome - Hypertelorism - Macrocephaly [wikidoc.org]

Craniometaphyseal dysplasia MedGen UID: 82702 •Concept ID: C0265292 • Congenital Abnormality Craniometadiaphyseal dysplasia (CRMDD) is characterized clinically by macrocephaly with frontal prominence, dental hypoplasia, and increased bone fragility. [ncbi.nlm.nih.gov]

[…] syndrome Axial Skull and face Craniosynostosis Scaphocephaly Oxycephaly Trigonocephaly Craniofacial dysostosis Crouzon syndrome Hypertelorism Hallermann–Streiff syndrome Treacher Collins syndrome other Macrocephaly Platybasia Craniodiaphyseal dysplasia Dolichocephaly [en.wikipedia.org]

Axial Skull and face Craniosynostosis : Scaphocephaly Oxycephaly Trigonocephaly Craniofacial dysostosis : Crouzon syndrome Hypertelorism Hallermann–Streiff syndrome Treacher Collins syndrome other: Macrocephaly Platybasia Craniodiaphyseal dysplasia Dolichocephaly [ipfs.io]

[…] and deformations of musculoskeletal system (Q65-Q79, 754-756) Limbs hip: Dislocation of hip/Hip dysplasia - Upington disease feet (Club foot, Flat feet, Pes cavus) systemic dislocations Larsen syndrome head, face, spine and chest: skull, face and jaw (Dolichocephaly [wikidoc.org]

[…] dislocation Congenital knee dislocation foot deformity varus Club foot Pigeon toe valgus Flat feet Pes cavus Rocker bottom foot Hammer toe Either / both fingers and toes Polydactyly / Syndactyly Webbed toes Arachnodactyly Cenani–Lenz syndactylism Ectrodactyly Brachydactyly [en.wikipedia.org]

Congenital knee dislocation foot deformity : varus Club foot Pigeon toe valgus Flat feet Pes cavus Rocker bottom foot Hammer toe Either / both fingers and toes Polydactyly / Syndactyly webbed toes Arachnodactyly Cenani–Lenz syndactylism Ectrodactyly Brachydactyly [ipfs.io]

MedGen UID: 1644017 •Concept ID: C4551510 • Disease or Syndrome Carpenter syndrome is a rare autosomal recessive disorder with the cardinal features of acrocephaly with variable synostosis of the sagittal, lambdoid, and coronal sutures; peculiar facies; brachydactyly [ncbi.nlm.nih.gov]

limb, specified type NEC, thigh congenital Q65.81 ICD-10-CM Codes Adjacent To Q65.81 Q65.1 Congenital dislocation of hip, bilateral Q65.2 Congenital dislocation of hip, unspecified Q65.3 Congenital partial dislocation of hip, unilateral Q65.30 Congenital [icd10data.com]

The following references for the code Q65.81 are found in the index: - Coxa - valga (acquired) - See Also: Deformity, limb, specified type NEC, thigh; - congenital - Q65.81 Synonyms The following clinical terms are approximate synonyms or lay terms that [icdlist.com]

Carpenter syndrome 1 MedGen UID: 1644017 •Concept ID: C4551510 • Disease or Syndrome Carpenter syndrome is a rare autosomal recessive disorder with the cardinal features of acrocephaly with variable synostosis of the sagittal, lambdoid, and coronal sutures [ncbi.nlm.nih.gov]

It tends to go unnoticed until walking age is reached, when the deformity results in a leg length difference or abnormal gait pattern. [idoc.pub]

Clinically the patient presents with an abnormal gait and a leg length discrepancy. The limb is generally painless and a waddling gait is seen when the deformity is bilateral. [casesjournal.biomedcentral.com]