Catel–Manzke syndrome
Catel–Manzke syndrome is a rare genetic disorder characterized by distinctive abnormalities of the index fingers; the classic features of Pierre Robin syndrome; occasionally with additional physical findings.
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Catel–Manzke syndrome
Catel–Manzke syndrome is a rare genetic disorder characterized by distinctive abnormalities of the index fingers; the classic features of Pierre Robin syndrome; occasionally with additional physical findings.
has abstract
Catel–Manzke syndrome is a rar ...... additional physical findings.
@en
Das Catel-Manzke-Syndrom (CATM ...... ch V. Hermann Manzke (* 1933).
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La sindrome di Catel-Manzke, d ...... livello scheletrico e oculare.
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Zespół Catela-Manzkego (ang. C ...... nna Manzkego i Wernera Catela.
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998,790,841
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DiseasesDB
ICD
Q87.8
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MeshID
name
Catel–Manzke syndrome
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OMIM
Orphanet
synonyms
Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome
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wikiPageUsesTemplate
wordnet_type
subject
hypernym
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Catel–Manzke syndrome is a rar ...... additional physical findings.
@en
Das Catel-Manzke-Syndrom (CATM ...... ch V. Hermann Manzke (* 1933).
@de
La sindrome di Catel-Manzke, d ...... livello scheletrico e oculare.
@it
Zespół Catela-Manzkego (ang. C ...... nna Manzkego i Wernera Catela.
@pl
label
Catel-Manzke-Syndrom
@de
Catel–Manzke syndrome
@en
Sindrome di Catel-Manzke
@it
Zespół Catela-Manzkego
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name
Catel–Manzke syndrome
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