MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
COQ10D7 14562
SSS1 24562
sinus node disease, familial, autosomal recessive 24562
primary coenzyme Q10 deficiency 7 14562
apocrine breast carcinoma in situ 4562
breast apocrine carcinoma in situ 4562
sinus rhythm, congenital absence of 24562
coenzyme Q10 deficiency, primary, 7 14562
coenzyme Q10 deficiency, primary, 7; COQ10D7 http://purl.obolibrary.org/obo/MONDO_0014562
coenzyme Q10 deficiency, primary, type 7 14562
SCN5A sick sinus syndrome 24562
neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome 14562
COQ4-related neonatal encephalomyopathy 14562
apocrine carcinoma in situ of breast 4562
apocrine carcinoma in situ of the breast 4562