Human Phenotype Ontology 
Grandparent Node:
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Abnormality of adrenal morphology (HP:0011732)help
Grandparent Node:
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Neoplasm of the endocrine system (HP:0100568)help
Parent Node:
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Neoplasm of the adrenal gland (HP:0100631)help
..Starting node
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Neoplasm of the adrenal medulla (HP:0100642)help
Term ID: 100642
Name: Neoplasm of the adrenal medulla
Synonym: Medullar adrenal neoplasia
Definition: The presence of a neoplasm of the adrenal medulla.
Comments:
Reference: HP:0100642
Genes and Diseases:
 
       Child Nodes:
........expandAdrenal pheochromocytoma (HP:0006748) help

 Sister Nodes: 
..expandNeoplasm of the adrenal cortex (HP:0100641) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100642HP:0100642Neoplasm of the adrenal medulla0CCND1 CL E G H5951582ORPHA:892Von Hippel-Lindau disease1
HP:0100642HP:0100642Neoplasm of the adrenal medulla0DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paraganglioma
HP:0100642HP:0100642Neoplasm of the adrenal medulla0DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma44
HP:0100642HP:0100642Neoplasm of the adrenal medulla0EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma112
HP:0100642HP:0100642Neoplasm of the adrenal medulla0FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paraganglioma301
HP:0100642HP:0100642Neoplasm of the adrenal medulla0KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paraganglioma202
HP:0100642HP:0100642Neoplasm of the adrenal medulla0MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paraganglioma84
HP:0100642HP:0100642Neoplasm of the adrenal medulla0MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paraganglioma4
HP:0100642HP:0100642Neoplasm of the adrenal medulla0NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paraganglioma1952
HP:0100642HP:0100642Neoplasm of the adrenal medulla0RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paraganglioma572
HP:0100642HP:0100642Neoplasm of the adrenal medulla0RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma572
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paraganglioma304
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paraganglioma55
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paraganglioma237
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHB CL E G H639010681OMIM:115310Paragangliomas 4237
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma237
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paraganglioma147
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHC CL E G H639110682OMIM:605373Paragangliomas 3147
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paraganglioma129
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHD CL E G H639210683OMIM:168000Paragangliomas 1129
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma129
HP:0100642HP:0100642Neoplasm of the adrenal medulla0SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paraganglioma
HP:0100642HP:0100642Neoplasm of the adrenal medulla0TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paraganglioma131
HP:0100642HP:0100642Neoplasm of the adrenal medulla0VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paraganglioma490
HP:0100642HP:0100642Neoplasm of the adrenal medulla0VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paraganglioma490
HP:0100642HP:0100642Neoplasm of the adrenal medulla0VHL CL E G H742812687ORPHA:892Von Hippel-Lindau disease490
HP:0100642HP:0006748Adrenal pheochromocytoma1CCND1 CL E G H5951582ORPHA:892Von Hippel-Lindau diseaseHP:0040282 - Frequent1
HP:0100642HP:0006748Adrenal pheochromocytoma1DLST CL E G H17432911ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent
HP:0100642HP:0006748Adrenal pheochromocytoma1DNMT3A CL E G H17882978ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040281 - Very frequent44
HP:0100642HP:0006748Adrenal pheochromocytoma1EPAS1 CL E G H20343374ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040281 - Very frequent112
HP:0100642HP:0006748Adrenal pheochromocytoma1FH CL E G H22713700ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent301
HP:0100642HP:0006748Adrenal pheochromocytoma1KIF1B CL E G H2309516636ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent202
HP:0100642HP:0006748Adrenal pheochromocytoma1MAX CL E G H41496913ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent84
HP:0100642HP:0006748Adrenal pheochromocytoma1MDH2 CL E G H41916971ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent4
HP:0100642HP:0006748Adrenal pheochromocytoma1NF1 CL E G H47637765ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent1952
HP:0100642HP:0006748Adrenal pheochromocytoma1RET CL E G H59799967ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent572
HP:0100642HP:0006748Adrenal pheochromocytoma1RET CL E G H59799967ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040281 - Very frequent572
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHA CL E G H638910680ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent304
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHAF2 CL E G H5494926034ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent55
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHB CL E G H639010681ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent237
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHB CL E G H639010681OMIM:115310Paragangliomas 4.237
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHB CL E G H639010681ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040281 - Very frequent237
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHC CL E G H639110682ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent147
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHC CL E G H639110682OMIM:605373Paragangliomas 3.147
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHD CL E G H639210683ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent129
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHD CL E G H639210683OMIM:168000Paragangliomas 1129
HP:0100642HP:0006748Adrenal pheochromocytoma1SDHD CL E G H639210683ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040281 - Very frequent129
HP:0100642HP:0006748Adrenal pheochromocytoma1SLC25A11 CL E G H840210981ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent
HP:0100642HP:0006748Adrenal pheochromocytoma1TMEM127 CL E G H5565426038ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent131
HP:0100642HP:0006748Adrenal pheochromocytoma1VHL CL E G H742812687ORPHA:29072Hereditary pheochromocytoma-paragangliomaHP:0040281 - Very frequent490
HP:0100642HP:0006748Adrenal pheochromocytoma1VHL CL E G H742812687ORPHA:276621Sporadic pheochromocytoma/secreting paragangliomaHP:0040281 - Very frequent490
HP:0100642HP:0006748Adrenal pheochromocytoma1VHL CL E G H742812687ORPHA:892Von Hippel-Lindau diseaseHP:0040282 - Frequent490


Genes (18) :CCND1 DLST DNMT3A EPAS1 FH KIF1B MAX MDH2 NF1 RET SDHA SDHAF2 SDHB SDHC SDHD SLC25A11 TMEM127 VHL

Diseases (6) :ORPHA:892 ORPHA:29072 ORPHA:276621 OMIM:115310 OMIM:605373 OMIM:168000
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.