Potter facies

Symptom Information:

Symptom ID: HPO:0002009
Synonyms:
Potter facies [OMIM:Potter facies]
Quality:
Cross references:
OMIM: "Potter facies" [OMIM:Potter facies]
Is a (Direct Parents):
HPO         Facial shape deformation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormal facial shape(HPO:0001999)
                   Facial shape deformation(HPO:0011334)
                      Potter facies(HPO:0002009)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive polycystic kidney disease (Orphanet:731)
Bilateral renal agenesis (Orphanet:1848)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
RENAL HYPODYSPLASIA/APLASIA 2 (OMIM:615721)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Renal tubular dysgenesis (Orphanet:3033)
Renal tubular dysgenesis of genetic origin (Orphanet:97369)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)