OBO ID: DOID:0080044
Term Name: hypochondrogenesis Search Ontology:
Synonyms:
Definition: An osteochondrodysplasia that has_material_basis_in a mutation in the COL2A1 gene which affects bone growth and results_in a small body, hydrops fetalis, and abnormal ossification located_in vertebral column or located_in pelvis. The disease has_symptom enlarged abdomen. (3)
References:
Ontology: Human Disease   ( DOID:0080044 )
Relationships
is a type of:
OTHER hypochondrogenesis PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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