Disease #06768 (DEDDFA (Developmental delay with or without dysmorphic facies and autism), OMIM:618454)

Official abbreviation DEDDFA
Name Developmental delay with or without dysmorphic facies and autism
OMIM ID 618454
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TRRAP
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00402812 Pat3 PM1, PM2, PM5, PP3, PP5 2-generation family, 1 affected, unaffected non carrier parents M no Mexico - - - - none DEDDFA iris coloboma, neurodevelopmental delay , hypotonia, seizures, microcephaly, highly arched eyebrow, medial cleft lip and palate, bilateral cryptorchidism. - TRRAP 1 1 Miriam Erandi Reyna-Fabián
00431542 213556 - - M likely Iraq Kurdish - - - - DEDDFA Global developmental delay, Synophrys, Depressed nasal bridge, Abnormality of the face TRRAP TRRAP 1 1 Andreas Laner
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