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All terms in MONDO

Label Id Description
bone dysplasia Moore type MONDO_0022586
bone dysplasia corpus callosum agenesis MONDO_0022587
blepharo naso facial syndrome van Maldergem type MONDO_0022580
methylcobalamin deficiency type cblG MONDO_0009609
methionine malabsorption syndrome MONDO_0009608
methionine adenosyltransferase deficiency MONDO_0009607
methemoglobinemia due to deficiency of methemoglobin reductase MONDO_0009606
methemoglobinemia type 4 MONDO_0009605
methemoglobin reductase deficiency MONDO_0009604
3-hydroxyisobutyryl-CoA hydrolase deficiency MONDO_0009603
valine metabolism disease MONDO_0037870
metaphyseal modeling abnormality, skin lesions, and spastic paraplegia MONDO_0009602
metaphyseal dysplasia without hypotrichosis MONDO_0009601
metaphyseal dysplasia, anetoderma, and optic atrophy MONDO_0009600
granulomatous disease, chronic, X-linked MONDO_0010600
microcephaly-micromelia syndrome MONDO_0009619
microcephaly-cardiomyopathy syndrome MONDO_0009618
microcephaly 1, primary, autosomal recessive MONDO_0009617
microcephalic primordial dwarfism, Toriello type MONDO_0009616
methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency MONDO_0009615