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1 OMIM reference -
1 associated gene
28 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Achondrogenesis type 1A
Hypoinsulinemic hypoglycemia and body hemihypertrophy

TRIP11 AKT2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
TRIP11
(0.63)
AKT2



Citations in the biomedical literature:


Achondrogenesis type 1A
TRIP11
Hypoinsulinemic hypoglycemia and body hemihypertrophy
AKT2



Achondrogenesis type 1A
Hypoinsulinemic hypoglycemia and body hemihypertrophy

Synonym(s):
- Achondrogenesis, Houston-Harris type

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C536015
External references:
1 OMIM reference -
No MeSH references

Achondrogenesis type 1A

Very frequent
- Abnormal / absent ossification
- Anteverted nares / nostrils
- Autosomal recessive inheritance
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Excess nuchal skin without pterygium colli
- Flat face
- Frontal bossing / prominent forehead
- Hydrops fetalis
- Hypoplastic lungs / pulmonary hypoplasia / agenesis
- Long philtrum
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Micrognathia / retrognathia / micrognathism / retrognathism
- Narrow rib cage / thorax
- Short limbs / micromelia / brachymelia
- Short neck
- Short rib cage / thorax
- Short stature / dwarfism / nanism
- Short / small nose
- Stillbirth / neonatal death

Frequent
- Inguinal / inguinoscrotal / crural hernia
- Mutiple fractures / bone fragility
- Polyhydramnios
- Rib structure anomalies
- Short foot / brachydactyly of toes
- Short hand / brachydactyly
- Umbilical hernia

Occasional
- Congenital cardiac anomaly / malformation / cardiopathy
- Cystic hygroma


Hypoinsulinemic hypoglycemia and body hemihypertrophy

(no data available)