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- B010ecd64d43c788e297009d83a6fa4fa hasDbXref "GARD:0000068" @default.
- B010ecd64d43c788e297009d83a6fa4fa hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B010ecd64d43c788e297009d83a6fa4fa type Axiom @default.
- B010ecd64d43c788e297009d83a6fa4fa annotatedProperty IAO_0000115 @default.
- B010ecd64d43c788e297009d83a6fa4fa annotatedSource MONDO_0007073 @default.
- B010ecd64d43c788e297009d83a6fa4fa annotatedTarget "A rare condition that primarily affects the craniofacial region and the limbs (arms and legs). People affected by this condition are often born with a short, incompletely developed tongue; absent or partially missing fingers and/or toes; abnormalities of the arms and/or legs; and an extremely small jaw. The severity of these physical abnormalities varies greatly among affected people, and children with this condition often have some, but not all, of the symptoms. The cause of Hanhart syndrome is not fully understood. Treatment depends on the signs and symptoms present in each person." @default.