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Otopalatodigital syndrome type 2
1 OMIM reference -
1 associated gene
43 signs/symptoms
PROTEIN INTERACTIONS: 1
Acute promyelocytic leukemia
1 OMIM reference -
7 associated genes
No signs/symptoms info
Otopalatodigital syndrome type 2
Acute promyelocytic leukemia

FLNA
(UniProt - OMIM)
 NABP1
(UniProt - OMIM)
NPM1
(UniProt - OMIM)
NUMA1
(UniProt - OMIM)
PML
(UniProt - OMIM)
RARA
(UniProt - OMIM)
STAT5B
(UniProt - OMIM)
ZBTB16
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLNA
(0.63)
NPM1


Citations in the biomedical literature:


Otopalatodigital syndrome type 2
FLNA
Acute promyelocytic leukemia
NABP1 NPM1 NUMA1 PML RARA STAT5B
ZBTB16



Otopalatodigital syndrome type 2
Acute promyelocytic leukemia

Synonym(s):
(no synonyms)

Synonym(s):
- Acute myeloblastic leukemia type 3
- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare neurologic disease
- Rare otorhinolaryngologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: x-linked dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C538089
External references:
1 OMIM reference -
1 MeSH reference: D015473
Otopalatodigital syndrome type 2

Very frequent
- Anodontia / oligodontia / hypodontia
- Bowed diaphysis / diaphyses / long bones
- Broad nose / nasal bridge
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Death in infancy
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Hearing loss / hypoacusia / deafness
- Hypertelorism
- Hypoplastic lungs / pulmonary hypoplasia / agenesis
- Large fontanelle / delayed fontanelle closure
- Narrow rib cage / thorax
- Prominent supraorbital ridge
- Short big toe
- Thumb hypoplasia / aplasia / absence
- X-linked recessive inheritance

Frequent
- Anomalies of spine, vertebrae and pelvis
- Camptodactyly of fingers
- Cardiac septal defect
- Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia
- Dense / thickened skull / calvarium / cranial / facial hyperostosis
- Elbow dislocation
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Fibula anomaly (excluding short) / absence / agenesis / hypoplasia / fibular ray anomaly
- Frontal sinus agenesis / anomaly
- Glossoptosis
- Hydrocephaly
- Hypospadias / epispadias / bent penis
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Metacarpal anomalies / Archibald's sign
- Micrognathia / retrognathia / micrognathism / retrognathism
- Omphalocele / exomphalos
- Osteosclerosis / osteopetrosis / bone condensation
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality
- Rib structure anomalies
- Short hand / brachydactyly
- Vertebral segmentation anomaly / hemivertebrae

Occasional
- Carpal bones fusion / synostosis
- Encephalocele / exencephaly
- Myelomeningocele
- Preaxial polydactyly of toes / big toe duplication
- Scoliosis
- Tarsal anomaly / fusion / synostosis


Acute promyelocytic leukemia

(no data available)