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searching for Hypochondrogenesis 2 found (14 total)

alternate case: hypochondrogenesis

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

600972; SLC26A2 Achondrogenesis type 1A; 200600; TRIP11 Achondrogenesis-hypochondrogenesis type 2; 200610; COL2A1 Achondroplasia; 100800; FGFR3 Achromatopsia-2;
Coiled-coil domain containing 42B (2,150 words) [view diff] exact match in snippet view article find links to article
chromosome 12 (12q24.13), which is linked to skeletal deformities, hypochondrogenesis, achondrogenesis, and kniest dysplasia. According to OMIM search chromosome