Crisponi syndrome
Crisponi syndrome (CS) is a severe disorder characterized by muscular contractions at birth, intermittent hyperthermia, facial abnormalities and camptodactyly
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Crisponi syndrome
Summary
Crisponi syndrome is a class of disease[1].
Key Facts
- Crisponi syndrome's instance of is recorded as class of disease[2].
- Crisponi syndrome's subclass of is recorded as cold-induced sweating syndrome[3].
- Crisponi syndrome's MeSH descriptor ID is recorded as C536214[4].
- Crisponi syndrome's OMIM ID is recorded as 601378[5].
- Crisponi syndrome's OMIM ID is recorded as 272430[6].
- Crisponi syndrome's Orphanet ID is recorded as 1545[7].
- Crisponi syndrome's genetic association is recorded as CRLF1[8].
- Crisponi syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1545[9].
- Crisponi syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_157820[10].
- Crisponi syndrome's UMLS CUI is recorded as C1832409[11].
- Crisponi syndrome's UMLS CUI is recorded as C1848947[12].
- Crisponi syndrome's ICD-10-CM is recorded as G90.8[13].
- Crisponi syndrome's Mondo ID is recorded as MONDO_0010091[14].
- Crisponi syndrome's ICD-11 ID is recorded as 1658600991[15].