| Disease Browser
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Parent Node:
 Jaw Abnormalities (D007569) | ..Starting node
.. Micrognathism (D008844)
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Child Nodes:
| | ........Baetz-Greenwalt syndrome (C537795) | | ........Bird headed dwarfism Montreal type (C535448) | | ........Cerebral Cavernous Malformations 2 (C566394) | | ........Cerebral Cavernous Malformations 3 (C566393) | | ........Cerebrocostomandibular Syndrome (C562538) | | ........Clavicular Hypoplasia, Zygomatic Arch Hypoplasia, and Micrognathia (C565729) | | ........Coffin-Siris syndrome (C536436) | | ........Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia (C564509) | | ........Crumpled helices and small mouth (C536217) | | ........Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia (C563344) | | ........Genee-Wiedemann syndrome (C537680) | | ........Genito palato cardiac syndrome (C537683) | | ........Ho Kaufman Mcalister syndrome (C538325) | | ........Limb Deficiencies, Distal, with Micrognathia (C565437) | | ........Meier-Gorlin syndrome (C538012) | | ........Milner Khallouf Gibson syndrome (C537473) | | ........Multiple Epiphyseal Dysplasia with Robin Phenotype (C563291) | | ........Schweitzer Kemink Graham syndrome (C536511) | | ........Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759) | | ........Yunis Varon syndrome (C536719) |
Sister Nodes: | ..Acrorenal mandibular syndrome (C535665)
| ..Agnathia-microstomia-synotia (C538059)
| ..Cleft Palate (D002972)  103
| ..Cleft Palate-Lateral Synechia Syndrome (C563047)
| ..Dysgnathia complex (C537996)
| ..External Ophthalmoplegia, Synergistic Divergence, Jaw Winking, and Oculocutaneous Hypopigmentation (C566509)
| ..GNATHODIAPHYSEAL DYSPLASIA (OMIM:166260)
| ..Hypoglossia-Hypodactylia (C566308)
| ..Marcus Gunn phenomenon (C535908)
| ..MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS (OMIM:613671)
| ..Micrognathism (D008844) 20
| ..Ophthalmomandibulomelic Dysplasia (C563501)
| ..Pierre Robin Syndrome (D010855) 18
| ..Prognathism (D011378) 4
| ..Retrognathia (D063173) 3
| ..Verloove-Vanhorick Brubakk syndrome (C536541)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 7212 |
| Name: | Micrognathism |
| Definition: | Abnormally small jaw. |
| Alternative IDs: | |
| ParentIDs: | MESH:D007569 |
| TreeNumbers: | C05.500.460.457 |C05.660.207.540.460.457 |C07.320.440.457 |C07.650.500.460.457 |C16.131.621.207.540.460.457 |C16.131.850.500.460.457 |
| Synonyms: | Congenital Micrognathia |Congenital Micrognathias |Congenital Micrognathism |Congenital Micrognathisms |Mandibular Micrognathia |Mandibular Micrognathias |Mandibular Micrognathism |Mandibular Micrognathisms |Micrognathia |Micrognathia, Congenital |Micrognathia, Ma |
| Slim Mappings: | Congenital abnormality|Mouth disease|Musculoskeletal disease |
| Reference: |
MedGen: D008844
MeSH: D008844
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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