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
single upper central incisor 7819
atypical dentin dysplasia due to SMOC2 deficiency 17819
trisomy 7p chromosome 7 C537819
solitary MEDIAN maxillary central incisor 7819
solitary median maxillary central incisor syndrome 7819
solitary MEDIAN maxillary central incisor; SMMCI http://purl.obolibrary.org/obo/MONDO_0007819
single central maxillary incisor 7819
postaxial, with median cleft of upper lip polydactyly C557819
chromosome 7, trisomy 7p C537819
oral-facial-digital syndrome, type v C557819
fibular agenesis-hypoplasia, oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome C567819
type v oral-facial-digital syndrome C557819
orofaciodigital syndrome, thurston type C557819
dentin dysplasia type 1 with microdontia and shape anomalies 17819
orofaciodigital syndrome v C557819