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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
13 OMIM references -
11 associated genes
20 signs/symptoms
Charcot-Marie-Tooth disease type 4D
Blackfan-Diamond anemia

NDRG1 RPL11
RPL15
RPL26
RPL35A
RPL5
RPS10
RPS17
RPS19
RPS24
RPS26
RPS7


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NDRG1
(0.73)
RPS26



Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 4D
NDRG1
Blackfan-Diamond anemia
RPL11 RPL15 RPL26 RPL35A RPL5 RPS10
RPS17 RPS19 RPS24 RPS26 RPS7



Charcot-Marie-Tooth disease type 4D
Blackfan-Diamond anemia

Synonym(s):
- CMT4D
- HMSN, Lom type
- Hereditary motor and sensory neuropathy, Lom type

Synonym(s):
- Aase syndrome
- Aase-Smith II syndrome
- Congenital PRCA
- Congenital hypoplastic anemia, Blackfan-Diamond type
- Congenital pure red cell aplasia

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare hematologic disease
- Rare maxillo-facial surgical disease
- Rare oncologic disease
- Rare otorhinolaryngologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C535716
External references:
13 OMIM references -
1 MeSH reference: D029503

Blackfan-Diamond anemia

Very frequent
- Anaemia
- Cardiac rhythm disorder / arrhythmia
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Pallor

Frequent
- Anomalies of hands
- Asthenia / fatigue / weakness
- Autosomal dominant inheritance
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Facial pain / cephalalgia / migraine
- Late puberty / hypogonadism / hypogenitalism
- Macrocytic anemia
- Structural anomalies of the genital system
- Structural anomalies of the kidney and the urinary tract

Occasional
- Acute leukemia
- Autosomal recessive inheritance
- Flattened nose
- Neoplasms / tumors
- Short stature / dwarfism / nanism
- Short / small nose
- Thick lips


Charcot-Marie-Tooth disease type 4D

(no data available)