1. Mendelian
  2. Rare Diseases
  3. ANALBUMINEMIA; ANALBA

Congenital Analbuminemia

Table of contents:

Description

Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).

Genes related to Congenital Analbuminemia

  • ALB

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Congenital Analbuminemia

  • Neoplasm
  • Fatigue
  • Edema
  • Osteoporosis
  • Carcinoma
  • Small for gestational age
  • Hypotension
  • Hyperlipidemia
  • Atherosclerosis
  • Hypercholesterolemia

And another 4 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Congenital Analbuminemia Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Analbuminemia (sequence analysis of ALB gene).

By CGC Genetics (Portugal).

ALB
Specificity
100 %
Genes
100 %
Analbuminemia (sequence analysis of ALB gene).

By CGC Genetics (Portugal).

ALB
Specificity
100 %
Genes
100 %
ALB.

By Fulgent Genetics Fulgent Genetics (United States).

ALB
Specificity
100 %
Genes
100 %

You can get up to -5 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Symptoms Checker

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