Potter facies
Symptom Information:
Symptom ID: | HPO:0002009 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |