Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:100050	AARSKOG SYNDROME, AUTOSOMAL DOMINANT	—	—	—
OMIM	OMIM:100070	AORTIC ANEURYSM, FAMILIAL ABDOMINAL, 1; AAA1	—	—	—
OMIM	OMIM:100100	PRUNE BELLY SYNDROME; PBS	—	—	—
OMIM	OMIM:100200	ABDUCENS PALSY	—	—	—
OMIM	OMIM:100300	ADAMS-OLIVER SYNDROME 1; AOS1	—	—	—
OMIM	OMIM:100500	MOVED TO 200150	—	—	—
OMIM	OMIM:100600	ACANTHOSIS NIGRICANS	—	—	—
OMIM	OMIM:100650	ALDEHYDE DEHYDROGENASE 2 FAMILY; ALDH2	—	—	—
OMIM	OMIM:100675	ACETAMINOPHEN METABOLISM	—	—	—
OMIM	OMIM:100680	MOVED TO 100740	—	—	—
OMIM	OMIM:100700	ACHARD SYNDROME	—	—	—
OMIM	OMIM:100735	MOVED TO 142445	—	—	—
OMIM	OMIM:100800	ACHONDROPLASIA; ACH	—	—	—
OMIM	OMIM:100820	ACHOO SYNDROME	—	—	—
OMIM	OMIM:100900	MOVED TO 100880	—	—	—
OMIM	OMIM:101000	NEUROFIBROMATOSIS, TYPE II; NF2	—	—	—
OMIM	OMIM:101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III	—	—	—
OMIM	OMIM:101200	APERT SYNDROME	—	—	—
OMIM	OMIM:101400	SAETHRE-CHOTZEN SYNDROME; SCS	—	—	—
OMIM	OMIM:101600	PFEIFFER SYNDROME	—	—	—
OMIM	OMIM:101800	ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1	—	—	—
OMIM	OMIM:101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE	—	—	—
OMIM	OMIM:101840	ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT	—	—	—
OMIM	OMIM:101850	PALMOPLANTAR KERATODERMA, PUNCTATE TYPE III; PPKP3	—	—	—
OMIM	OMIM:101900	ACROKERATOSIS VERRUCIFORMIS; AKV	—	—	—