CODE	OMIM_HPO_ID	NAME
A1AT	OMIM_ICD:86	Alpha-1-antitrypsin Deficiency
COMP	OMIM_ICD:15	Complement Deficiency
DBA	OMIM_ICD:89	Constitutional Red Blood Cell Aplasia
HHT	OMIM_ICD:108	Hereditary Hemorrhagic Telangiectasia
HMSN	OMIM_ICD:113	Hereditary Motor and Sensory Neuropathy
MAR	OMIM_ICD:120	Marfan Syndrome
NF	OMIM_ICD:125	Neurofibromatosis
22Q	OMIM_ICD:129	22q Deletion Syndrome
PCKD	OMIM_ICD:132	Polycystic Kidney Disease
