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Congenital analbuminemia
1 associated gene
148 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
Epidermolytic palmoplantar keratoderma
Pachyonychia congenita
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Annular epidermolytic ichthyosis
B-cell chronic lymphocytic leukemia
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Epidermolytic ichthyosis
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Immunodeficiency due to an early component of complement deficiency
Leber congenital amaurosis
Localized epidermolysis bullosa simplex
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Fanconi anemia
Zonular cataract
Hyperlipidemia type 3
Lipoprotein glomerulopathy
Sea-blue histiocytosis
Aspartylglucosaminuria
Catecholaminergic polymorphic ventricular tachycardia
Congenital factor VII deficiency
3M syndrome
Acute necrotizing encephalopathy of childhood
Adenosine monophosphate deaminase deficiency
Alexander disease type I
Alexander disease type II
Amyotrophic lateral sclerosis type 4
Apolipoprotein A-I deficiency
Ataxia-telangiectasia
Ataxia-telangiectasia variant
Atrial stand still
Atypical hemolytic uremic syndrome with B factor anomaly
Atypical hemolytic uremic syndrome with H factor anomaly
Autosomal dominant spastic paraplegia type 4
Autosomal recessive centronuclear myopathy
Autosomal recessive epidermolysis bullosa simplex
Autosomal recessive limb-girdle muscular dystrophy type 2J
Autosomal recessive limb-girdle muscular dystrophy type 2S
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Autosomal recessive spastic paraplegia type 44
Becker muscular dystrophy
Behçet disease
Brugada syndrome
Cerebral sinovenous thrombosis
Cholesterol-ester transfer protein deficiency
Citrullinemia type II
Combined cervical dystonia
Congenital factor II deficiency
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect
Congenital nephrotic syndrome, Finnish type
Congenital reticular ichthyosiform erythroderma
Dense deposit disease
Dermatopathia pigmentosa reticularis
Dowling-Degos disease
Duchenne muscular dystrophy
Early-onset myopathy with fatal cardiomyopathy
Epidermolysis bullosa simplex with circinate migratory erythema
Familial acute necrotizing encephalopathy
Familial afibrinogenemia
Familial amyloid polyneuropathy
Familial amyloidosis, Finnish type
Familial apolipoprotein C-II deficiency
Familial atrial fibrillation
Familial congenital mirror movements
Familial drusen
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Familial multinodular goiter
Familial pancreatic carcinoma
Familial progressive cardiac conduction defect
Familial renal amyloidosis due to Apolipoprotein AI variant
Familial renal amyloidosis due to Apolipoprotein AII variant
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Familial sick sinus syndrome
Fetal and neonatal alloimmune thrombocytopenia
Fibronectin glomerulopathy
Generalized epilepsy - paroxysmal dyskinesia
Hereditary angioedema type 1
Hereditary angioedema type 2
Hereditary breast and ovarian cancer syndrome
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type
Hereditary chronic pancreatitis
Hereditary proximal myopathy with early respiratory failure
Ichthyosis hystrix of Curth-Macklin
Idiopathic ventricular fibrillation, not Brugada type
Immunodeficiency with factor H anomaly
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Inflammatory myofibroblastic tumor
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
Keratosis palmoplantaris striata
Left ventricular noncompaction
Mantle cell lymphoma
Milroy disease
Naegeli-Franceschetti-Jadassohn syndrome
Neonatal intrahepatic cholestasis due to citrin deficiency
Non-progressive cerebellar ataxia with intellectual deficit
Ovarian malignant Sertoli-Leydig cell tumor
Pelizaeus-Merzbacher-like due to GJC2 mutation
Pigmented paravenous retinochoroidal atrophy
Pleuropulmonary blastoma family tumor susceptibility syndrome
Primary systemic amyloidosis
Recurrent Neisseria infections due to factor D deficiency
Retinitis pigmentosa
Romano-Ward syndrome
Senior-Loken syndrome
Severe intellectual deficit and progressive spastic paraplegia
Spinocerebellar ataxia with axonal neuropathy type 2
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
Tibial muscular dystrophy
Transthyretin-related familial amyloid cardiomyopathy
White sponge nevus
ZASP-related myofibrillar myopathy
Alpha-crystallinopathy
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Autosomal dominant methemoglobinemia
Congenital atransferrinemia
Cystic fibrosis
Donnai-Barrow syndrome
Fatal infantile hypertonic myofibrillar myopathy
Hb Bart's hydrops fetalis
Hemoglobin H disease
Laron syndrome
Posterior polar cataract
Short stature due to partial GHR deficiency
Young adult-onset Parkinsonism
Gräsbeck-Imerslund disease
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Spinocerebellar ataxia type 12
Amyotrophic lateral sclerosis
Cataract-microcornea syndrome
Hyperinsulinism due to HNF1A deficiency
MODY syndrome
Nuclear cataract
Progressive retinal dystrophy due to retinol transport defect
Very long chain acyl-CoA dehydrogenase deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
ALB P02768103600
No signs/symptoms info available.