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

There is 0 pattern entry.

Label
Id
MDDGA5 13157
muscle-eye-brain-FKRP related 13157
Gorham's disease 3157
Gorham-Stout syndrome 3157
essential osteolysis 3157
massive osteolysis 3157
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5 13157
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5; MDDGA5 http://purl.obolibrary.org/obo/MONDO_0013157
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5 13157
Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-Related http://purl.obolibrary.org/obo/MONDO_0013157
disappearing bone disease 3157
phantom bone disease 3157
Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related 13157
fibular hypoplasia scapulo pelvic dysplasia absent 23157
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