Disease #00560 (MARTS1 (Martsolf syndrome, type 1), OMIM:212720)

Official abbreviation MARTS1
Name Martsolf syndrome, type 1
OMIM ID 212720
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene RAB3GAP2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-07-24 14:22:05 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00363164 family PubMed: Aligianis 2006 4-generation family, 3 affected sibs (F, 2M), unaffected heterozygous carrier parent/relatives F;M yes Pakistan - - - - - MARTS1 see paper; ..., no intrauterine growth retardation, postnatal growth retardation; birth OF 34cm; postnatal microcephaly; no seizures; truncal hypotonia; limb spasticity and spastic cerebral palsy; 3y-speech; 3y-walking; congenital cataracts?, microphthalmia; brachycephaly; no distinct dysmorphic features, no maxillary retrusion or pouting lips; hirsutism; female no genital abnormalities/male micropenis, cryptorchidism; large ears; CT brain normal RAB3GAP2 RAB3GAP2 1 3 Johan den Dunnen
00435409 264057 - - F likely ? (unknown) - - - - - MARTS1 High palate, Retrognathia, Hearing impairment, Cataract, Developmental cataract, Hypotelorism, Synophrys, Single transverse palmar crease, Dystonia RAB3GAP2 RAB3GAP2 1 1 Andreas Laner
00467591 - - - - - China - - - - - MARTS1 - RAB3GAP2 RAB3GAP2 1 1 Xuemei Tan
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