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
CCMS 7301
CCM syndrome 7301
CEREBROCOSTOMANDIBULAR syndrome 7301
cerebro-costo-mandibular syndrome 7301
cerebrocostomandibular syndrome 7301
griscelli syndrome, cutaneous and neurologic type C537301
CEREBROCOSTOMANDIBULAR syndrome; CCMS http://purl.obolibrary.org/obo/MONDO_0007301
lactic acidosis, congenital infantile, due to LAD deficiency C573012
type 1 griscelli syndrome C537301
cutaneous and neurologic type griscelli syndrome C537301
rib Gap defects with micrognathia 7301
congenital infantile, due to LAD deficiency lactic acidosis C573012
lactic acidosis due to lipoamide dehydrogenase deficiency C573012
griscelli syndrome type 1 C537301
griscelli syndrome, type 1 C537301