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- Fibrochondrogenesis abstract "Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues.It is a lethal rhizomelic (malformations which result in short, underdeveloped limbs) form of dwarfism, exhibiting both skeletal dysplasia (malformations of bone) and fibroblastic dysplasia (abnormal development of fibroblasts, specialized cells that make up fibrous connective tissue, which plays a role in the formation of cellular structure and promotes healing of damaged tissues). Death caused by complications of fibrochondrogenesis occurs in infancy.".
- Fibrochondrogenesis diseasesdb "34294".
- Fibrochondrogenesis icd10 "Q77.9".
- Fibrochondrogenesis icd9 "756.4".
- Fibrochondrogenesis omim "228520".
- Fibrochondrogenesis wikiPageID "19771817".
- Fibrochondrogenesis wikiPageRevisionID "591307214".
- Fibrochondrogenesis diseasesdb "34294".
- Fibrochondrogenesis hasPhotoCollection Fibrochondrogenesis.
- Fibrochondrogenesis icd "756.4".
- Fibrochondrogenesis icd "Q77.9".
- Fibrochondrogenesis name "Fibrochondrogenesis".
- Fibrochondrogenesis omim "228520".
- Fibrochondrogenesis subject Category:Autosomal_recessive_disorders.
- Fibrochondrogenesis subject Category:Congenital_disorders.
- Fibrochondrogenesis subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Fibrochondrogenesis subject Category:Rare_diseases.
- Fibrochondrogenesis type Abnormality114501726.
- Fibrochondrogenesis type Abstraction100002137.
- Fibrochondrogenesis type Anomaly114505821.
- Fibrochondrogenesis type Attribute100024264.
- Fibrochondrogenesis type AutosomalRecessiveDisorders.
- Fibrochondrogenesis type BirthDefect114465048.
- Fibrochondrogenesis type Condition113920835.
- Fibrochondrogenesis type CongenitalDisorders.
- Fibrochondrogenesis type Defect114464005.
- Fibrochondrogenesis type Disease114070360.
- Fibrochondrogenesis type Disorder114052403.
- Fibrochondrogenesis type GeneticDisease114151139.
- Fibrochondrogenesis type GeneticDisordersWithOMIMButNoGene.
- Fibrochondrogenesis type IllHealth114052046.
- Fibrochondrogenesis type Illness114061805.
- Fibrochondrogenesis type Imperfection114462666.
- Fibrochondrogenesis type PathologicalState114051917.
- Fibrochondrogenesis type PhysicalCondition114034177.
- Fibrochondrogenesis type State100024720.
- Fibrochondrogenesis type Disease.
- Fibrochondrogenesis type AilmentCondition.
- Fibrochondrogenesis type Situation.
- Fibrochondrogenesis comment "Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues.It is a lethal rhizomelic (malformations which result in short, underdeveloped limbs) form of dwarfism, exhibiting both skeletal dysplasia (malformations of bone) and fibroblastic dysplasia (abnormal development of fibroblasts, specialized cells that make up fibrous connective tissue, which plays a role in the formation of cellular structure and promotes healing of damaged tissues). ".
- Fibrochondrogenesis label "Fibrochondrogenesis".
- Fibrochondrogenesis label "Fibrocondrogénesis".
- Fibrochondrogenesis sameAs Fibrocondrogénesis.
- Fibrochondrogenesis sameAs m.04q1zh7.
- Fibrochondrogenesis sameAs Q5446460.
- Fibrochondrogenesis sameAs Q5446460.
- Fibrochondrogenesis sameAs Fibrochondrogenesis.
- Fibrochondrogenesis wasDerivedFrom Fibrochondrogenesis?oldid=591307214.
- Fibrochondrogenesis isPrimaryTopicOf Fibrochondrogenesis.
- Fibrochondrogenesis name "Fibrochondrogenesis".