autosomal

999	recessive
855	syndrome
701	congenital
674	deficiency
660	mutations
656	dysplasia
646	abnormalities
636	chromosome
634	autoimmune
634	mutation

previous:	AUTOSAR
next:	autosome
random:	HCPS

More distant neighbors

gene disorder disease atrophy abnormality symptoms chromosomal allele abnormal neurological anemia genes degenerative alleles asymptomatic disorders homozygous lesions heterozygous syndromes inflammation chronic dystrophy infection bowel colitis phenotype liver idiopathic fibrosis adrenal tumors hypoplasia cystic symptom malformations degeneration genetic thyroid

Back