Descriptor English: | Orofaciodigital Syndromes | ||||||
Descriptor Spanish: |
Síndromes Orofaciodigitales
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Descriptor Portuguese: | Síndromes Orofaciodigitais | ||||||
Descriptor French: | Syndromes oro-facio-digitaux | ||||||
Entry term(s): |
Dysplasia Linguofacialis Gorlin Psaume Syndrome Gorlin-Psaume Syndrome Mohr Syndrome Oral Facial Digital Syndrome, Type I Oral Facial Digital Syndrome, Type II Oral-Facial-Digital Syndrome Oral-Facial-Digital Syndrome, Type I Oral-Facial-Digital Syndrome, Type II Oro-Facio-Digital Syndrome Orodigitofacial Dysostosis Orodigitofacial Syndrome Orofaciodigital Syndrome Orofaciodigital Syndrome I Orofaciodigital Syndrome II Orofaciodigital Syndrome IIs Orofaciodigital Syndrome Is Papillon Leage and Psaume Syndrome Papillon-Leage and Psaume Syndrome Syndrome, Gorlin-Psaume Syndrome, Mohr Syndrome, Orofaciodigital Syndromes, Orofaciodigital |
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Tree number(s): |
C05.116.099.370.652 C05.660.207.700 C16.131.077.676 C16.131.260.830.670 C16.131.621.207.700 C16.320.180.830.670 C16.320.714 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D009958 | ||||||
Scope note: | Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait. |
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Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | 79; was OROFACIODIGITAL SYNDROME see under ABNORMALITIES, MULTIPLE 1975-78 |
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Online Note: | use OROFACIODIGITAL SYNDROMES to search OROFACIODIGITAL SYNDROME 1966-78(as Prov 1966-74) |
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History Note: | 79; was OROFACIODIGITAL SYNDROME see under ABNORMALITIES, MULTIPLE 1975-78; was OROFACIODIGITAL SYNDROME 1964-74 (Prov) |
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DeCS ID: | 10135 | ||||||
Unique ID: | D009958 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1991/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2016/06/30 |
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Orofaciodigital Syndromes
- Preferred
Papillon-Leage and Psaume Syndrome
- Narrower
Mohr Syndrome
- Narrower
Concept UI |
M0015438 |
Scope note | Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait. |
Preferred term | Orofaciodigital Syndromes |
Entry term(s) |
Dysplasia Linguofacialis Oral-Facial-Digital Syndrome Oro-Facio-Digital Syndrome Orodigitofacial Dysostosis Orodigitofacial Syndrome Orofaciodigital Syndrome Syndrome, Orofaciodigital Syndromes, Orofaciodigital |
Concept UI |
M0015440 |
Preferred term | Papillon-Leage and Psaume Syndrome |
Entry term(s) |
Gorlin Psaume Syndrome Gorlin-Psaume Syndrome Oral Facial Digital Syndrome, Type I Oral-Facial-Digital Syndrome, Type I Orofaciodigital Syndrome I Orofaciodigital Syndrome Is Papillon Leage and Psaume Syndrome Syndrome, Gorlin-Psaume |
Concept UI |
M0015437 |
Preferred term | Mohr Syndrome |
Entry term(s) |
Oral Facial Digital Syndrome, Type II Oral-Facial-Digital Syndrome, Type II Orofaciodigital Syndrome II Orofaciodigital Syndrome IIs Syndrome, Mohr |
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