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
spastic paraplegia 6, autosomal dominant; SPG6 http://purl.obolibrary.org/obo/MONDO_0010878
hereditary optic Atrophies 43878
COL4A1 or COL4A2-related cerebral angiopathy 18788
COL4A1 or COL4A2-related cerebral angiopathy with ischemic tendancy 18789
COL4A1 or COL4A2-related cerebral small vessel disease 18788
COL4A1 or COL4A2-related cerebral small vessel disease with ischemic tendancy 18789
Cornelia de Lange-like syndrome 19878
uterine corpus Mullerian adenosarcoma 2878
uterine corpus Müllerian adenosarcoma 2878
ichthyosis hystrix Rheydt type 18781
NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA 32878
abscess, intra abdominal D018784
intra abdominal abscess D018784
uterine body adenosarcoma 2878
uterine corpus adenosarcoma 2878