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- B331fb9657fb80f02290235edd1c7dffe hasDbXref "Orphanet:435938" @default.
- B331fb9657fb80f02290235edd1c7dffe type Axiom @default.
- B331fb9657fb80f02290235edd1c7dffe annotatedProperty IAO_0000115 @default.
- B331fb9657fb80f02290235edd1c7dffe annotatedSource MONDO_0018569 @default.
- B331fb9657fb80f02290235edd1c7dffe annotatedTarget "X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiovascular septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding." @default.