All terms in HP
Label | Id | Description |
---|---|---|
decreased length | PATO_0000574 | [A length quality which is relatively small.] |
increased height | PATO_0000570 | [A height which is relatively high.] |
Vaginal neoplasm | HP_0100650 | [A tumor (abnormal growth of tissue) of the vagina.] |
Genital neoplasm | HP_0010787 | [A tumor (abnormal growth of tissue) of the genital system.] |
Type I diabetes mellitus | HP_0100651 | [A chronic condition in which the pancreas produces little or no insulin. Type I diabetes mellitus is manifested by the sudden onset of severe hyperglycemia with rapid progression to diabetic ketoacidosis unless treated with insulin.] |
Retrobulbar optic neuritis | HP_0100654 | [Optic neuritis that occurs in the section of the optic nerve located behind the eyeball.] |
Optic neuritis | HP_0100653 | [Inflammation of the optic nerve.] |
Abnormality of the optic nerve | HP_0000587 | [Abnormality of the optic nerve.] |
Thoracoabdominal wall defect | HP_0100656 | [Failure to close of the chest and abdominal wall likely caused by the failure of the ventral wall to close during week 4 of development.] |
Abdominal wall defect | HP_0010866 | [An incomplete closure of the abdominal wall.] |
Cellulitis | HP_0100658 | [A bacterial infection and inflammation of the skin und subcutaneous tissues.] |
Thoracoabdominal eventration | HP_0100657 | [Congenital protrusion of the abdominal or thoracic viscera, usually with a defect of the sternum and ribs as well as of the abdominal walls.] |
Abnormality of the cerebral vasculature | HP_0100659 | |
serum albumin (human) | PR_P02768 | [A serum albumin that is encoded in the genome of human.] |
serum albumin | PR_000003918 | [A protein that is a translation product of the human ALB gene or a 1:1 ortholog thereof.] |
ALB (human) | gene_symbol_report | [A protein coding gene ALB in human.] |
regulation of cytokine production | GO_0001817 | [Any process that modulates the frequency, rate, or extent of production of a cytokine.] |
gene | SO_0000704 | [A region (or regions) that includes all of the sequence elements necessary to encode a functional transcript. A gene may include regulatory regions, transcribed regions and/or other functional sequence regions.] |
protein_coding | SO_0000010 | |
Esophageal duplication | HP_0100681 | [A developmental disorder in which there is a duplication of a portion of the muscle and submucosa of the esophagus without epithelial duplication.] |