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5 OMIM references -
5 associated genes
35 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
1 OMIM reference -
1 associated gene
22 signs/symptoms
Ear-patella-short stature syndrome
ADULT syndrome

CDC6 TP63
CDT1
ORC1
ORC4
ORC6


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CDT1
(0.63)
TP63



Citations in the biomedical literature:


Ear-patella-short stature syndrome
CDC6 CDT1 ORC1 ORC4 ORC6
ADULT syndrome
TP63



Ear-patella-short stature syndrome
ADULT syndrome

Synonym(s):
- Meier-Gorlin syndrome

Synonym(s):
- Acro-dermato-ungual-lacrimal-tooth syndrome
- Pigment anomaly - ectrodactyly - hypodontia

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare odontologic disease
- Rare skin disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
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: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
5 OMIM references -
1 MeSH reference: C538012
External references:
1 OMIM reference -
1 MeSH reference: C538052


COMMON
SIGNS
- Breast tissue / mammary gland absence / aplasia


Ear-patella-short stature syndrome
ADULT syndrome

Very frequent
- Autosomal recessive inheritance
- Delayed bone age
- Epiphyseal anomaly
- External auditory canal atresia / stenosis / agenesis
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Hyperextensible joints / articular hyperlaxity
- Hypoplastic mandibula / partial absence of the mandibula
- Intrauterine growth retardation
- Microcephaly
- Micrognathia / retrognathia / micrognathism / retrognathism
- Microstomia / little mouth
- Microtia / cryptomicrotia / anotia / external auditory canal / pinnae aplasia / hypoplasia
- Narrowed / gracile diaphysis / diaphyses / long bones / dolichostenomelia
- Short stature / dwarfism / nanism
- Undescended / ectopic testes / cryptorchidia / unfixed testes

Frequent
- Camptodactyly of fingers
- Clavicle absent / abnormal
- Clinodactyly of fifth finger
- Clitoris / labia majora / labia minora / female external genitalia hypoplasia
- Craniostenosis / craniosynostosis / sutural synostosis
- Female pseudohermaphrodism / virilisation / clitoridomegaly
- High vaulted / narrow palate
- Hypoplastic maxillary bones / zygomatic bones / maxillary hypoplasia
- Low set ears / posteriorly rotated ears
- Patella absent / abnormal (excluding luxation)
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Rib structure anomalies

Occasional
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Elbow dislocation
- Hearing loss / hypoacusia / deafness
- Hypospadias / epispadias / bent penis
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Micropenis / small penis / agenesis
- Thick lips


Very frequent
- Anomalies of eyelids, eyelashes and lacrimal system
- Anomalies of teeth and dentition
- Chronic skin infection / ulcerations / ulcers / cancrum
- Dry / squaly skin / exfoliation
- Dysplastic / thick / grooved fingernails
- Dysplastic / thick / grooved toenails
- Excessive freckling
- Fine hair
- Nails anomalies
- Oligodactyly / ectrodactyly of toes
- Pigmented naevi / naevus pigmentosus / lentigo
- Syndactyly of fingers / interdigital palm
- Syndactyly of toes
- Thin skin

Frequent
- Alopecia
- Hypoplastic / absent nipples
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
- Tooth shape anomaly

Occasional
- Broad nose / nasal bridge
- Face / facial anomalies
- High nasal bridge