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 neuromuscular transmission http://purl.obolibrary.org/obo/HP_0003398
Abnormality of neuronal migration http://purl.obolibrary.org/obo/HP_0002269
Abnormality of neurotransmitter metabolism http://purl.obolibrary.org/obo/HP_0012535
Abnormality of neutrophil http://purl.obolibrary.org/obo/HP_0001874
Abnormality of neutrophil morphology http://purl.obolibrary.org/obo/HP_0011992
Abnormality of neutrophil morphology in cerebrospinal fluid http://purl.obolibrary.org/obo/HP_0410310
Abnormality of neutrophil morphology in CSF http://purl.obolibrary.org/obo/HP_0410310
Abnormality of neutrophil physiology http://purl.obolibrary.org/obo/HP_0011990
Abnormality of neutrophils http://purl.obolibrary.org/obo/HP_0001874
Abnormality of nose hair http://purl.obolibrary.org/obo/HP_0040057
Abnormality of occipitofrontalis muscle http://purl.obolibrary.org/obo/HP_0040172
Abnormality of ocular abduction http://purl.obolibrary.org/obo/HP_0011347
Abnormality of ocular smooth pursuit http://purl.obolibrary.org/obo/HP_0000617
Abnormality of odontoid tissue http://purl.obolibrary.org/obo/HP_3000050
Abnormality of oesophagus physiology http://purl.obolibrary.org/obo/HP_0025270