Pitt-Hopkins syndrome
rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent hyperventilation followed by apnea
Press Enter · cited answer in seconds
0 sources
Pitt-Hopkins syndrome
Summary
Pitt-Hopkins syndrome is a rare disease[1]. It draws 413 Wikipedia views per month (rare_disease category, ranking #142 of 627).[2]
Key Facts
- Pitt-Hopkins syndrome's instance of is recorded as rare disease[3].
- Pitt-Hopkins syndrome's instance of is recorded as class of disease[4].
- Pitt-Hopkins syndrome is a type of syndrome[5].
- Pitt-Hopkins syndrome is a type of genetic syndromic intellectual disability[6].
- Pitt-Hopkins syndrome is a type of genetic disease[7].
- Pitt-Hopkins syndrome is a type of autosomal dominant disease[8].
- Pitt-Hopkins syndrome's Commons category is recorded as Pitt–Hopkins syndrome[9].
- Pitt-Hopkins syndrome's ICD-9-CM is recorded as 758.5[10].
- Pitt-Hopkins syndrome's NCI Thesaurus ID is recorded as C129872[11].
- Pitt-Hopkins syndrome's health specialty is recorded as psychiatry[12].
- Pitt-Hopkins syndrome's genetic association is recorded as TCF4[13].
- Pitt-Hopkins syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060488[14].
- Pitt-Hopkins syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060488[15].
- Pitt-Hopkins syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2896[16].
- Pitt-Hopkins syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Pitt-Hopkins syndrome draws 413 Wikipedia views per month (rare_disease category, ranking #142 of 627).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[18] It is known by 9 alternative names across languages and contexts.[19]