From: <doe...@us...> - 2010-02-15 17:45:30
|
Revision: 3116 http://obo.svn.sourceforge.net/obo/?rev=3116&view=rev Author: doelkens Date: 2010-02-15 17:44:48 +0000 (Mon, 15 Feb 2010) Log Message: ----------- added annotation for Teunissen-Cremers and removed faulty angelman-file Modified Paths: -------------- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-105830_Angelman.tab Added Paths: ----------- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-184460_Teunissen-Cremers.tab Removed Paths: ------------- phenotype-commons/annotations/OMIM/by-disease/annotated/~$M-105830_Angelman.tab Modified: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-105830_Angelman.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-105830_Angelman.tab 2010-02-15 17:06:07 UTC (rev 3115) +++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-105830_Angelman.tab 2010-02-15 17:44:48 UTC (rev 3116) @@ -1,4 +1,4 @@ -Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add'l Entity Name Mode of inheritance ID Mode of inheritance Name Age of onset ID Age of onset Name Evidence Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add'l Entity Name Mode of Inheritance ID Mode of Inheritance Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000158 Macroglossia PCS 25% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000181 Macrostomia PCS 25% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000303 Mandibular prognathia PCS 25% ISBN-13:978-0721606156 17.02.2009 @@ -8,16 +8,16 @@ MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000635 Blue irides PCS 88% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000639 Nystagmus PCS 7.5 % ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000687 Widely spaced teeth PCS 25% ISBN-13:978-0721606156 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000749 Paroxysmal bursts of laughter common MIM:105830 17.02.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000749 Paroxysmal bursts of laughter PCS common MIM:105830 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001010 Hypopigmentation of the skin PCS 39% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001250 Seizures PCS 86% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001252 Muscular hypotonia PCS 25% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001347 Hyperreflexia PCS 7.5 % ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001420 Isolated cases isolated vs spordic??? 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001513 Obesity occasional MIM:105830 17.02.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001513 Obesity PCS occasional MIM:105830 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0001617 Absent speech PCS 100% ISBN-13:978-0721606156 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002019 Constipation occasional MIM:105830 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002022 Feeding difficulties occasional MIM:105830 17.02.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002019 Constipation PCS occasional MIM:105830 17.02.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002022 Feeding difficulties PCS occasional MIM:105830 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002130 Delayed motor milestones PCS 100% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002136 Broad-based gait HPO:sdoelken hallmark 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002214 Blond hair PCS 65% ISBN-13:978-0721606156 17.02.2009 @@ -25,17 +25,17 @@ MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002312 Clumsiness HPO:sdoelken hallmark 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002353 EEG abnormalities PCS 92% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0002650 Scoliosis PCS 7.5 % ISBN-13:978-0721606156 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0005469 Occipital plagiocephaly common MIM:105830 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0005484 Microcephaly, postnatal common MIM:105830 17.02.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0005469 Occipital plagiocephaly PCS common MIM:105830 17.02.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0005484 Microcephaly, postnatal PCS common MIM:105830 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0006823 Mild cortical atrophy on ct or mri PCS 33% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0006887 Mental retardation, progressive PCS 100% ISBN-13:978-0721606156 17.02.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0007240 Progressive gait ataxia PCS 100% ISBN-13:978-0721606156 17.02.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED del15q11.2-q13mat 15q11.2-q13 HP:0003745 Sporadic 70% MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED imprinting defect 15q11.2-q13 (maternal methylated by default) 15q11.2-q13 HP:0003745 Sporadic 2% MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED UBE3A / wt UBE3A HP:0003745 Sporadic 25% MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED papaternal uniparental disomy 15q11.2-q13 15q11.2-q13 HP:0003745 Sporadic 2% MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt MECP2 HP:0003745 Sporadic rare MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000752 Hyperactivity common MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED UBE3A / wt; imprinting center mutations UBE3A, 15q11.2-q13 HP:0000006 Autosomal dominant inheritance rare MIM:105830 03.12.2009 -MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0006979 Sleep-wake cycle disturbance occasional MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED del15q11.2-q13mat 15q11.2-q13 HP:0003745 Sporadic PCS 70% MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED imprinting defect 15q11.2-q13 (maternal methylated by default) 15q11.2-q13 HP:0003745 Sporadic PCS 2% MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED UBE3A / wt UBE3A HP:0003745 Sporadic PCS 25% MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED papaternal uniparental disomy 15q11.2-q13 15q11.2-q13 HP:0003745 Sporadic PCS 2% MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt MECP2 HP:0003745 Sporadic PCS rare MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0000752 Hyperactivity PCS common MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED UBE3A / wt; imprinting center mutations UBE3A, 15q11.2-q13 HP:0000006 Autosomal dominant inheritance PCS rare MIM:105830 03.12.2009 +MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0006979 Sleep-wake cycle disturbance PCS occasional MIM:105830 03.12.2009 MIM:105830 ANGELMAN SYNDROME ANGELMAN SYNDROME CHROMOSOME REGION, INCLUDED MECP2 / wt; UBE3A / wt, 15q11.2-q13 / wt MECP2, UBE3A, 15q11.2-q13 HP:0006887 Mental retardation, progressive PCS 100% ISBN-13:978-0721606156 19.01.2010 Added: phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-184460_Teunissen-Cremers.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-184460_Teunissen-Cremers.tab (rev 0) +++ phenotype-commons/annotations/OMIM/by-disease/annotated/MIM-184460_Teunissen-Cremers.tab 2010-02-15 17:44:48 UTC (rev 3116) @@ -0,0 +1,14 @@ +Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Entity ID Entity Name Quality ID Quality Name Add'l Entity ID Add'l Entity Name Mode of Inheritance ID Mode of Inheritance Name Age of Onset ID Age of Onset Name Evidence Frequency Abnormal ID Abnormal Name Description Orthologs Pub Date Created +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0000006 Autosomal dominant inheritance IEA MIM:184460 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0003189 Long nose PCS frequent PMID:10069712 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0000405 Hearing loss, conductive HP:0003601 Onset in utero or at birth PCS hallmark MIM:184460 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0000466 Limited neck range of motion PCS 3/6 PMID:10069712; PMID:2319886 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0000540 Hypermetropia PCS hallmark MIM:184460 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0001770 Toe syndactyly PCS frequent PMID:10069712; PMID:2319886 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0002949 Fused cervical vertebrae PCS 2/5 PMID:2319886 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0007943 Congenital stapes ankylosis PCS hallmark MIM:184460 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0009651 Broad phalanges of the thumb PCS hallmark MIM:184460 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0009882 Hypoplasia of the distal phalanges of the hand PCS common PMID:2319886 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0010055 Broad hallux PCS hallmark MIM:184460 17.02.2009 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0000430 Hypoplastic nasal alae PCS frequent PMID:10069712 15.02.2010 +MIM:184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES SYNDACTYLY TEUNISSEN-CREMERS SYNDROME STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM MIM:602991 NOGGIN, MOUSE, HOMOLOG OF MIM:602991 / wt NOG HP:0009765 Long columella PCS frequent PMID:2319886 15.02.2010 Deleted: phenotype-commons/annotations/OMIM/by-disease/annotated/~$M-105830_Angelman.tab =================================================================== (Binary files differ) This was sent by the SourceForge.net collaborative development platform, the world's largest Open Source development site. |