Human Phenotype Ontology 
Grandparent Node:
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Mortality/Aging (HP:0040006)help
Parent Node:
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Age of death (HP:0011420)help
..Starting node
..expand
Death in adolescence (HP:0011421)help
Term ID: 11421
Name: Death in adolescence
Synonym: Death in adolescence
Definition: Death during adolescence, the period between childhood and adulthood (roughly between the ages of 10 and 19 years).
Comments:
Reference: HP:0011421
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDeath in childhood (HP:0003819) help
..expandDeath in early adulthood (HP:0100613) help
..expandDeath in infancy (HP:0001522) help
..expandNeonatal death (HP:0003811) help
..expandStillbirth (HP:0003826) help
..expandSudden death (HP:0001699) 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:0011421HP:0011421Death in adolescence0ACTN2 CL E G H88164OMIM:612158Cardiomyopathy, dilated, 1aa, with or without left ventricular noncompaction307
HP:0011421HP:0011421Death in adolescence0COX8A CL E G H13512294OMIM:619059MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 15; MC4DN151
HP:0011421HP:0011421Death in adolescence0DSP CL E G H18323052OMIM:605676Cardiomyopathy, dilated, with woolly hair and keratoderma747
HP:0011421HP:0011421Death in adolescence0ERCC4 CL E G H20723436OMIM:610965XFE progeroid syndrome158
HP:0011421HP:0011421Death in adolescence0EXOC8 CL E G H14937124659OMIM:619076NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND BRAIN ATROPHY; NEDMISB1
HP:0011421HP:0011421Death in adolescence0FGA CL E G H22433661OMIM:202400Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included47
HP:0011421HP:0011421Death in adolescence0FGB CL E G H22443662OMIM:202400Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included62
HP:0011421HP:0011421Death in adolescence0FGG CL E G H22663694OMIM:202400Afibrinogenemia, congenitalhypofibrinogenemia, congenital, included34
HP:0011421HP:0011421Death in adolescence0GFAP CL E G H26704235OMIM:203450Alexander disease188
HP:0011421HP:0011421Death in adolescence0IL6ST CL E G H35726021OMIM:619751STUVE-WIEDEMANN SYNDROME 2; STWS2
HP:0011421HP:0011421Death in adolescence0MADD CL E G H85676766OMIM:619004DEEAH SYNDROME; DEEAH5
HP:0011421HP:0011421Death in adolescence0MDFIC CL E G H2996928870OMIM:620014
HP:0011421HP:0011421Death in adolescence0MFSD2A CL E G H8487925897OMIM:616486Microcephaly 15, primary, autosomal recessive5
HP:0011421HP:0011421Death in adolescence0OAS1 CL E G H49388086OMIM:618042Pulmonary alveolar proteinosis with hypogammaglobulinemia2
HP:0011421HP:0011421Death in adolescence0PET100 CL E G H10013180140038OMIM:619055MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 12; MC4DN126
HP:0011421HP:0011421Death in adolescence0PSMB8 CL E G H56969545OMIM:256040Proteasome-associated autoinflammatory syndrome 1 and digenic forms20
HP:0011421HP:0011421Death in adolescence0SATB1 CL E G H630410541OMIM:619229KOHLSCHUTTER-TONZ SYNDROME-LIKE; KTZSL
HP:0011421HP:0011421Death in adolescence0TPI1 CL E G H716712009OMIM:615512Triosephosphate isomerase deficiency28


Genes (18) :ACTN2 COX8A DSP ERCC4 EXOC8 FGA FGB FGG GFAP IL6ST MADD MDFIC MFSD2A OAS1 PET100 PSMB8 SATB1 TPI1

Diseases (16) :OMIM:612158 OMIM:619059 OMIM:605676 OMIM:610965 OMIM:619076 OMIM:202400 OMIM:203450 OMIM:619751 OMIM:619004 OMIM:620014 OMIM:616486 OMIM:618042 OMIM:619055 OMIM:256040 OMIM:619229 OMIM:615512
 

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