CODE	OMIM_HPO_ID	NAME
HHT	OMIM_ICD:108	Hereditary Hemorrhagic Telangiectasia
MAR	OMIM_ICD:120	Marfan Syndrome
FD	OMIM_ICD:118	Familial Dysautonomia
AS	OMIM_ICD:121	Alport Syndrome
HMSN	OMIM_ICD:113	Hereditary Motor and Sensory Neuropathy
HEME	OMIM_ICD:83	Hemachromatosis
PE	OMIM_ICD:99	Primary Erythermalgia
A1AT	OMIM_ICD:86	Alpha-1-antitrypsin Deficiency
PCKD	OMIM_ICD:132	Polycystic Kidney Disease
SCA	OMIM_ICD:138	Sickle Cell Anemia
