Human Phenotype Ontology 
..Starting node
..expandAnhydramnios (HP:0025700)help
Term ID: 25700
Name: Anhydramnios
Synonym:
Definition: A complete or near-complete lack of amniotic fluid surrounding a fetus. This finding can be observed sonographically in the third trimesters if the deepest pocket of amniotic fluid is less than or equal to 2 cm.
Comments:
Reference: HP:0025700
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:0025700HP:0025700Anhydramnios0GFRA1 CL E G H26744243OMIM:6198871
HP:0025700HP:0025700Anhydramnios0ITGA8 CL E G H85166144OMIM:191830Renal hypodysplasia/aplasia 14
HP:0025700HP:0025700Anhydramnios0TCTN2 CL E G H7986725774OMIM:613885Meckel syndrome, type 876


Genes (3) :GFRA1 ITGA8 TCTN2

Diseases (3) :OMIM:619887 OMIM:191830 OMIM:613885
 

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