OMIM
Db Link Name Definition Comment Is a
OMIM OMIM:106400 ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSIS
OMIM OMIM:106500 ANNULAR ERYTHEMA
OMIM OMIM:106600 TOOTH AGENESIS, SELECTIVE, 1; STHAG1
OMIM OMIM:106700 TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1; TAPVR1
OMIM OMIM:106750 ANONYCHIA WITH FLEXURAL PIGMENTATION
OMIM OMIM:106900 ANONYCHIA-ECTRODACTYLY
OMIM OMIM:106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY
OMIM OMIM:106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES
OMIM OMIM:107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6
OMIM OMIM:107100 ANORECTAL ANOMALIES
OMIM OMIM:107200 ANOSMIA, ISOLATED CONGENITAL; ANIC
OMIM OMIM:107240 MOVED TO 116930
OMIM OMIM:107250 ANTERIOR SEGMENT DYSGENESIS 1; ASGD1
OMIM OMIM:107253 REMOVED FROM DATABASE
OMIM OMIM:107290 ANTIPYRINE METABOLISM
OMIM OMIM:107320 ANTIPHOSPHOLIPID SYNDROME, FAMILIAL
OMIM OMIM:107410 SERPIN PEPTIDASE INHIBITOR, CLADE A, MEMBER 2, PSEUDOGENE; SERPINA2P
OMIM OMIM:107440 ANTIVIRAL STATE REPRESSOR, REGULATOR OF; AVRR
OMIM OMIM:107460 MOVED TO 107450
OMIM OMIM:107480 TOWNES-BROCKS SYNDROME 1; TBS1
OMIM OMIM:107500 AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION
OMIM OMIM:107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA
OMIM OMIM:107600 APLASIA CUTIS CONGENITA, NONSYNDROMIC; ACC
OMIM OMIM:107601 MOVED TO 100300
OMIM OMIM:107640 APNEA, CENTRAL SLEEP