HP-PA-20210116 Find_IDs Find_Terms Annotation
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created at 2021-01-16 06:16:13 UTC
updated at 2024-09-23 16:21:39 UTC
terms for phenotypic abnormality as defined in HP.
The entries were initially sourced from the HP version 2020-12-07 as stored in BioPortal.
34,075 entries
Label
Id
Abnormality of cartilage of nasal septum http://purl.obolibrary.org/obo/HP_3000034
Abnormality of cartilage of nose http://purl.obolibrary.org/obo/HP_0030027
Abnormality of cartilage of septum of nose http://purl.obolibrary.org/obo/HP_3000034
Abnormality of cation homeostasis http://purl.obolibrary.org/obo/HP_0010929
Abnormality of CD4+ T cells http://purl.obolibrary.org/obo/HP_0005407
Abnormality of cell physiology http://purl.obolibrary.org/obo/HP_0011017
Abnormality of cells of the erythroid lineage http://purl.obolibrary.org/obo/HP_0012130
Abnormality of cells of the granulocytic lineage http://purl.obolibrary.org/obo/HP_0012135
Abnormality of cells of the lymphoid lineage http://purl.obolibrary.org/obo/HP_0004332
Abnormality of cells of the megakaryocyte lineage http://purl.obolibrary.org/obo/HP_0012143
Abnormality of central motor conduction http://purl.obolibrary.org/obo/HP_0012079
Abnormality of central motor function http://purl.obolibrary.org/obo/HP_0011442
Abnormality of central nervous system electrophysiology http://purl.obolibrary.org/obo/HP_0030178
Abnormality of central retinal artery http://purl.obolibrary.org/obo/HP_3000032
Abnormality of central sensory function http://purl.obolibrary.org/obo/HP_0011730