Human Phenotype Ontology 
Grandparent Node:
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Abnormality of skin morphology (HP:0011121)help
Parent Node:
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Pallor (HP:0000980)help
..Starting node
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Anemic pallor (HP:0001017)help
Term ID: 1017
Name: Anemic pallor
Synonym: Anaemic pallor
Definition: A type of pallor that is secondary to the presence of anemia.
Comments:
Reference: HP:0001017
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001017HP:0001017Anemic pallor0ALAS2 CL E G H212397OMIM:300751Anemia, sideroblastic, X-linked72
HP:0001017HP:0001017Anemic pallor0BMPR1A CL E G H6571076ORPHA:329971Generalized juvenile polyposis/juvenile polyposis coliHP:0040282 - Frequent385
HP:0001017HP:0001017Anemic pallor0ENG CL E G H20223349ORPHA:329971Generalized juvenile polyposis/juvenile polyposis coliHP:0040282 - Frequent186
HP:0001017HP:0001017Anemic pallor0FANCA CL E G H21753582OMIM:227650Fanconi anemia.340
HP:0001017HP:0001017Anemic pallor0FANCC CL E G H21763584OMIM:227645Fanconi anemia, complementation group C.410
HP:0001017HP:0001017Anemic pallor0FANCD2 CL E G H21773585OMIM:227646Fanconi anemia, complementation group D2.147
HP:0001017HP:0001017Anemic pallor0FANCE CL E G H21783586OMIM:600901Fanconi anemia, complementation group E.73
HP:0001017HP:0001017Anemic pallor0SMAD4 CL E G H40896770ORPHA:329971Generalized juvenile polyposis/juvenile polyposis coliHP:0040282 - Frequent504


Genes (8) :ALAS2 BMPR1A ENG FANCA FANCC FANCD2 FANCE SMAD4

Diseases (6) :OMIM:300751 ORPHA:329971 OMIM:227650 OMIM:227645 OMIM:227646 OMIM:600901
 

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