Homer

Gene HMID	Gene Symbol	Organ Specificity	DiseaseID	Disease Name	Related Organ
HM05279	C11orf73	pharynx	MESH:D005355	Fibrosis
HM05279	C11orf73	pharynx	MESH:D014605	Uveitis	eye
HM05279	C11orf73	pharynx	MESH:D007638	Keratoconjunctivitis Sicca	eye
HM05279	C11orf73	pharynx	MESH:D005885	Gingival Hyperplasia
HM05279	C11orf73	pharynx	MESH:D006973	Hypertension	lung
HM05279	C11orf73	pharynx	MESH:D006973	Hypertension	heart
HM05279	C11orf73	pharynx	MESH:D006973	Hypertension	blood vessel
HM05279	C11orf73	pharynx	MESH:D008664	Metal Metabolism, Inborn Errors	skin
HM05279	C11orf73	pharynx	MESH:D008664	Metal Metabolism, Inborn Errors	muscle
HM05279	C11orf73	pharynx	MESH:D008664	Metal Metabolism, Inborn Errors	liver
HM05279	C11orf73	pharynx	MESH:D008664	Metal Metabolism, Inborn Errors	kidney
HM05279	C11orf73	pharynx	MESH:D009402	Nephrosis, Lipoid	kidney
HM05279	C11orf73	pharynx	MESH:D006457	Hemoglobinuria, Paroxysmal
HM05279	C11orf73	pharynx	MESH:D014985	Xerophthalmia	eye
HM05279	C11orf73	pharynx	MESH:D007674	Kidney Diseases	ureter
HM05279	C11orf73	pharynx	MESH:D007674	Kidney Diseases	pituitary
HM05279	C11orf73	pharynx	MESH:D007674	Kidney Diseases	kidney
HM05279	C11orf73	pharynx	MESH:D011565	Psoriasis	skin
HM05279	C11orf73	pharynx	MESH:D009404	Nephrotic Syndrome	kidney

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