Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:104130	ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY	—	—	—
OMIM	OMIM:104200	ALPORT SYNDROME, AUTOSOMAL DOMINANT	—	—	—
OMIM	OMIM:104222	MOVED TO 104219	—	—	—
OMIM	OMIM:104250	ALPHA-2C-ADRENERGIC RECEPTOR; ADRA2C	—	—	—
OMIM	OMIM:104290	ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1	—	—	—
OMIM	OMIM:104300	ALZHEIMER DISEASE; AD	—	—	—
OMIM	OMIM:104310	ALZHEIMER DISEASE 2; AD2	—	—	—
OMIM	OMIM:104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM	—	—	—
OMIM	OMIM:104400	AMELIA AND TERMINAL TRANSVERSE HEMIMELIA	—	—	—
OMIM	OMIM:104500	AMELOGENESIS IMPERFECTA, TYPE IB; AI1B	—	—	—
OMIM	OMIM:104510	AMELOGENESIS IMPERFECTA, TYPE IV; AI4	—	—	—
OMIM	OMIM:104530	AMELOGENESIS IMPERFECTA, TYPE IA; AI1A	—	—	—
OMIM	OMIM:104570	AMELOONYCHOHYPOHIDROTIC SYNDROME	—	—	—
OMIM	OMIM:104600	AMENORRHEA-GALACTORRHEA SYNDROME	—	—	—
OMIM	OMIM:104740	MOVED TO 602414	—	—	—
OMIM	OMIM:105120	AMYLOIDOSIS, FINNISH TYPE	—	—	—
OMIM	OMIM:105150	CEREBRAL AMYLOID ANGIOPATHY, CST3-RELATED	—	—	—
OMIM	OMIM:105200	AMYLOIDOSIS, FAMILIAL VISCERAL	—	—	—
OMIM	OMIM:105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED	—	—	—
OMIM	OMIM:105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1	—	—	—
OMIM	OMIM:105300	AMYOTROPHIC DYSTONIC PARAPLEGIA	—	—	—
OMIM	OMIM:105400	AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1	—	—	—
OMIM	OMIM:105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1	—	—	—
OMIM	OMIM:105550	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1; FTDALS1	—	—	—
OMIM	OMIM:105563	ANAL SPHINCTER DYSPLASIA; ASDP	—	—	—