Costello syndrome
syndrome characterized by craniofacial dysmorphology, cardiac defects, mild intellectual disability, and high birth weight followed by a failure to thrive and developmental delays
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Costello syndrome
Summary
Costello syndrome is a designated intractable/rare disease[1]. It draws 57 Wikipedia views per month (designated_intractable_rare_disease category, ranking #130 of 201).[2]
Key Facts
- Costello syndrome's image is recorded as Costello syndrome facial manifestation 17-year-old female.png[3].
- Costello syndrome's instance of is recorded as designated intractable/rare disease[4].
- Costello syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- Costello syndrome's instance of is recorded as rare disease[6].
- Costello syndrome's instance of is recorded as class of disease[7].
- Costello syndrome's subclass of is recorded as autosomal dominant disease[8].
- Costello syndrome's subclass of is recorded as genetic syndromic intellectual disability[9].
- Costello syndrome's subclass of is recorded as polymalformative genetic syndrome with increased risk of developing cancer[10].
- Costello syndrome's subclass of is recorded as dermis elastic tissue disorder[11].
- Costello syndrome's subclass of is recorded as hypertrophic cardiomyopathy[12].
- Costello syndrome's subclass of is recorded as Moyamoya syndrome[13].
- Costello syndrome's subclass of is recorded as Noonan syndrome and Noonan-related syndrome[14].
- Costello syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[15].
- Costello syndrome's subclass of is recorded as malformation syndrome with skin/mucosae involvement[16].
- Costello syndrome's subclass of is recorded as RASopathy[17].
- Costello syndrome's Commons category is recorded as Costello syndrome[18].
- Costello syndrome's MeSH descriptor ID is recorded as D056685[19].
- Costello syndrome's OMIM ID is recorded as 218040[20].
- Costello syndrome's DiseasesDB is recorded as 32846[21].
- Costello syndrome's Freebase ID is recorded as /m/09md0z[22].
- Costello syndrome's KEGG ID is recorded as H01747[23].
- Costello syndrome's GeneReviews ID is recorded as NBK1507[24].
- Costello syndrome's MeSH tree code is recorded as C05.660.207.219[25].
- Costello syndrome's MeSH tree code is recorded as C16.131.077.256[26].
- Costello syndrome's MeSH tree code is recorded as C16.320.188[27].
Why It Matters
Costello syndrome draws 57 Wikipedia views per month (designated_intractable_rare_disease category, ranking #130 of 201).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] It is known by 8 alternative names across languages and contexts.[29]