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Figure 1 | BMC Bioinformatics

Figure 1

From: Inherited disorder phenotypes: controlled annotation and statistical analysis for knowledge mining from gene lists

Figure 1

OMIM Clinical Synopsis section for the Phenylketonuria disease associated with the Phenylalanine Hydroxylase(PAH) human gene and with Mental retardation Neurologic phenotype. 261600: MIM (Mendelian Inheritance in Man) ID of the Phenylketonuria disease; +: in OMIM a plus sign before a MIM number entry indicates that the entry contains the description of a gene of known sequence and a phenotype; Neuro: Neurologic, GI: Gastrointestinal, Misc: Miscellaneous, Lab: Laboratory phenotype locations.

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BMC Bioinformatics

ISSN: 1471-2105

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