Micrognathia, mild

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Micrognathia, mild (in some patients) [OMIM:Micrognathia, mild (in some patients)]
Mild micrognathia [OMIM:Mild micrognathia]
Quality:
Cross references:
OMIM: "Micrognathia, mild" [OMIM:Micrognathia, mild]
OMIM: "Micrognathia, mild (in some patients)" [OMIM:Micrognathia, mild (in some patients)]
OMIM: "Mild micrognathia" [OMIM:Mild micrognathia]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cohen syndrome (Orphanet:193)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Hypertelorism-microtia-facial clefting syndrome (Orphanet:2213)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
Microcephalic primordial dwarfism, Toriello type (Orphanet:2643)
RENAL AND MULLERIAN DUCT HYPOPLASIA (OMIM:266810)