Description
Radial dysplasia inclusion criteria (37640)
•	Bilateral radial dysplasia, OR
•	Unilateral radial dysplasia with positive family history, parental consanguinity or additional syndromic features (such as at least one additional structural malformation, height/length or head circumference >3SDs from the mean, dysmorphism, moderate or worse intellectual disability or autism spectrum disorder)

Radial dysplasia exclusion criteria (37640)
•	Known genetic cause
•	Known teratogenic cause

Prior genetic testing guidance (37640)
- Results should have been reviewed for all genetic tests undertaken, including disease-relevant genes in exome sequencing data. The patient is not eligible if they have a molecular diagnosis for their condition. 
- Genetic testing should continue according to routine local practice for this phenotype regardless of recruitment to the project; results of these tests must be submitted via the ‘Genetic investigations’ section of the data capture tool to allow comparison of WGS with current standard testing.  

PLEASE NOTE: The sensitivity of WGS compared to current diagnostic genetic testing has not yet been established. It is therefore important that tests which are clinically indicated under local standard practice continue to be carried out.

Radial dysplasia prior genetic testing genes (37640)
Testing of the following genes should be carried out PRIOR TO RECRUITMENT where this is in line with current local practice:
- aCGH or equivalent
- Fanconi breakage testing (if features suggestive of Fanconi anaemia)
- TBX5 (if phenotype suggestive of Holt-Oram syndrome)
- RBM8A (if aCGH or clinical features suggestive of TAR syndrome)

Closing statement (37640)
These requirements will be kept under continual review during the main programme and may be subject to change.

Note that although GeneAdviser list TBX1 and TBX2 in their exome panel for Holt-Oram Syndrome, TBX1 and TBX2 are not listed in the four main sources as being associated with this disorder, so TBX1 and TBX2 have not currently been added to the panel.
Panel Activity

11 reviewers

  • Ellen McDonagh (Genomics England Curator)

    Group: Other
    Workplace: Other

  • Richard Scott (Genomics England Curator)

    Group: Other
    Workplace: Other

  • Ana Beleza (Bristol Regional Genetics Service)

    Group: Other NHS organisation
    Workplace: NHS clinical service

  • Sarah Leigh (Genomics England Curator)

    Group: Other
    Workplace: Other

  • Rebecca Foulger (Genomics England curator)

    Group: Other
    Workplace: Other

  • Louise Daugherty (Genomics England Curator)

    Group: Other
    Workplace: Other

  • BRIDGE consortium (NIHRBR-RD)

    Group: Other
    Workplace: Other

  • Helen Brittain (Genomics England Curator)

    Group: Other
    Workplace: Other

  • Eleanor Williams (Genomics England Curator)

    Group: Other
    Workplace: Other

  • Zornitza Stark (Australian Genomics)

    Group: Other
    Workplace: Other clinical service

  • Arina Puzriakova (Genomics England Curator)

    Group: Other
    Workplace: Other

60 Entities

60 reviewed, 47 green

List Entity Reviews Mode of inheritance Details
60 Entitiess
Green Green List (high evidence)
BRCA2
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group D1, OMIM:605724
Tags
Green Green List (high evidence)
BRIP1
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group J, OMIM:609054
Tags
Green Green List (high evidence)
ERCC4
4 reviews
3 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group Q, 615272
Tags
Green Green List (high evidence)
ESCO2
3 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Roberts syndrome, 268300
  • radial aplasia
  • absence of radii, SC phocomelia syndrome, 269000
Tags
Green Green List (high evidence)
FANCA
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group A, 227650
Tags
Green Green List (high evidence)
FANCB
4 reviews
1 green 		X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Eligibility statement prior genetic testing
  • Emory Genetics Laboratory
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • VACTERL Association with Hydrocephalus
  • VACTERL-Hydrocephalus Syndrome
  • Vacterl Association, X-Linked, With Or Without Hydrocephalus
  • Fanconi Anemia, Complementation Group B
  • Fanconi anemia, complementation group B, 300514
  • Fanconi Anemia, X-Linked
  • Fanconi Anemia Type B
Tags
Green Green List (high evidence)
FANCC
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group C, 227645
Tags
Green Green List (high evidence)
FANCD2
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group D2, 227646
Tags
Green Green List (high evidence)
FANCE
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group E, 600901
Tags
Green Green List (high evidence)
FANCF
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group F, 603467
Tags
Green Green List (high evidence)
FANCG
2 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group G, 614082
Tags
Green Green List (high evidence)
FANCI
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group I, 609053
Tags
Green Green List (high evidence)
FANCL
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group L, 614083
Tags
Green Green List (high evidence)
FGF10
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • LADD syndrome, 149730
  • Limb defects most often involved the thumbs, ranging from total aplasia to hypoplastic, digitalized, triphalangeal, and duplicated thumbs
  • short radius
Tags
Green Green List (high evidence)
FGFR2
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • LADD syndrome, 149730
  • Limb defects most often involved the thumbs, ranging from total aplasia to hypoplastic, digitalized, triphalangeal, and duplicated thumbs
  • short radius
Tags
Green Green List (high evidence)
FGFR3
3 reviews
2 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • LADD syndrome, 149730
  • Limb defects most often involved the thumbs, ranging from total aplasia to hypoplastic, digitalized, triphalangeal, and duplicated thumbs
  • short radius
Tags
Green Green List (high evidence)
FIG4
3 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Yunis Varon syndrome OMIM:216340
  • Yunis-Varon syndrome MONDO:0008995
Tags
Green Green List (high evidence)
FLNA
4 reviews
1 green 		X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Frontometaphyseal dysplasia 1, OMIM:305620
  • Melnick-Needles syndrome, OMIM:309350
  • Otopalatodigital syndrome, type I, OMIM:311300
  • Otopalatodigital syndrome, type II, OMIM:304120
  • Terminal osseous dysplasia, OMIM:300244
Tags
Green Green List (high evidence)
HDAC8
3 reviews
1 green 		X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Cornelia de Lange syndrome 5, 300882
Tags
Green Green List (high evidence)
HOXA13
4 reviews
3 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Hand-foot-uterus syndrome, 140000
Tags
Green Green List (high evidence)
KCNH1
2 reviews
1 green 1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Temple-Baraitser syndrome, 611816
  • Hypoplasia of terminal phalanges
Tags
Green Green List (high evidence)
LMBR1
5 reviews
1 green 		BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Laurin-Sandrow syndrome,135750
  • Triphalangeal thumb type I,174500
  • Triphalangeal Thumb-Polysyndactyly Syndrome
Tags
Green Green List (high evidence)
NIPBL
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Cornelia de Lange syndrome 1, 122470
  • CDLS1
  • Dislocation of the radial head
  • upper limb anomalies
Tags
Green Green List (high evidence)
PALB2
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group N, 610832
Tags
Green Green List (high evidence)
RBM8A
5 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Emory Genetics Laboratory
  • Expert list
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Thrombocytopenia-absent radius syndrome, 274000
Tags
Green Green List (high evidence)
RECQL4
3 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Emory Genetics Laboratory
  • Expert list
  • Expert Review Green
  • Other
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Baller-Gerold syndrome, OMIM:218600
  • RAPADILINO syndrome, OMIM:266280
  • Rothmund-Thomson syndrome, type 2, OMIM:268400
Tags
Green Green List (high evidence)
RPL11
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 7, 612562
  • thumb abnormalities
  • hypoplastic thumb
Tags
Green Green List (high evidence)
RPL35A
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 5, 612528
  • upper limb malformation
Tags
Green Green List (high evidence)
RPL5
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 6, 612561
  • thumb abnormalities
Tags
Green Green List (high evidence)
RPS10
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 9, 613308
  • upper limb malformation
Tags
Green Green List (high evidence)
RPS17
2 reviews
2 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 4, 612527
Tags
Green Green List (high evidence)
RPS19
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 1, 105650
  • Mild radial hypoplasia
  • Hypoplastic thumbs
  • Absent thumbs
  • Triphalangeal thumbs
Tags
Green Green List (high evidence)
RPS24
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 3, 610629
  • upper limb malformation
Tags
Green Green List (high evidence)
RPS26
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 10, 613309
  • upper limb malformation
Tags
Green Green List (high evidence)
RPS7
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Diamond-Blackfan anemia 8, 612563
  • upper limb malformation
Tags
Green Green List (high evidence)
SALL1
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
  • UKGTN
Phenotypes
  • Townes Brocks syndrome (Renal-Ear-Anal-Radial syndrome), 107480
Tags
Green Green List (high evidence)
SALL4
4 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
  • Other
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Duane-radial ray syndrome, 607323
  • IVIC syndrome, 147750
Tags
Green Green List (high evidence)
SF3B4
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Acrofacial dysostosis 1, Nager type, 154400
Tags
Green Green List (high evidence)
SHOX
5 reviews
2 green 		BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Langer mesomelic dysplasia, OMIM:249700 (PR)
  • Leri-Weill dyschondrosteosis, OMIM:127300 (PD)
  • Short stature, idiopathic familial, OMIM:300582
  • Dorsolateral bowed, short radii
  • Bowing and curving of radius
  • Radioulnar shortening
Tags
  • Pseudoautosomal region 1
Green Green List (high evidence)
SLX4
2 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group P, 613951
Tags
Green Green List (high evidence)
SMC1A
4 reviews
2 green 		X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Cornelia de Lange syndrome 2, OMIM:300590
  • Cornelia de Lange syndrome 2, MONDO:0010370
Tags
Green Green List (high evidence)
SMC3
5 reviews
2 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Cornelia de Lange syndrome 3, 610759
Tags
Green Green List (high evidence)
TBX3
3 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Ulnar-mammary syndrome, 181450
  • Hypoplastic/absent/deformed radius
Tags
Green Green List (high evidence)
TBX5
3 reviews
2 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Holt-Oram syndrome,142900
Tags
Green Green List (high evidence)
UBE2T
4 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Green
  • Other
Phenotypes
  • Fanconi Anemia, Complementation Group T, 616435
Tags
Green Green List (high evidence)
WNT7A
3 reviews
1 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
  • Other
Phenotypes
  • Ulna and fibula, absence of, with severe limb deficiency, 276820
  • Short, bowed radii
  • absence of a radius
  • Fuhrmann syndrome, 228930
Tags
Green Green List (high evidence)
ZIC3
2 reviews
 X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert list
  • Expert Review Green
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • VACTERL association, X-linked 314390
Tags
Amber Amber List (moderate evidence)
PTEN
3 reviews
1 green 1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Other
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • VATER association with macrocephaly and ventriculomegaly,276950
  • VACTERL ASSOCIATION WITH HYDROCEPHALUS
  • VACTERL-H
Tags
Amber Amber List (moderate evidence)
RAD21
6 reviews
3 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Other
Phenotypes
  • Cornelia de Lange syndrome 4, OMIM:614701
Tags
Amber Amber List (moderate evidence)
RAD51C
3 reviews
2 green 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert list
  • Expert Review Amber
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi anemia, complementation group O 613390
Tags
  • watchlist
Amber Amber List (moderate evidence)
RPL15
4 reviews
2 green 1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Amber
  • Other
Phenotypes
  • ?Diamond-Blackfan anemia 12
  • upper limb malformation
  • Triphalangeal thumbs
Tags
  • watchlist
Amber Amber List (moderate evidence)
RPL26
3 reviews
1 green 1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Amber
  • Other
Phenotypes
  • Diamond-Blackfan anemia 11
  • Hypoplasia or aplasia of radius, unilateral
  • Absent thumb, bilateral
Tags
  • watchlist
Amber Amber List (moderate evidence)
RPS29
4 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Other
Phenotypes
  • Diamond-Blackfan anemia 13
Tags
  • watchlist
Red Red List (low evidence)
CREBBP
2 reviews
 MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Other
Phenotypes
  • Rubinstein-Taybi syndrome 1, 180849
Tags
Red Red List (low evidence)
DACT1
1 review
1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
  • Other
Phenotypes
  • ?Townes-Brocks syndrome 2,617466
  • TBS2
Tags
Red Red List (low evidence)
FANCM
4 reviews
1 green 1 red 		BIALLELIC, autosomal or pseudoautosomal
Sources
  • Eligibility statement prior genetic testing
  • Expert Review Red
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
Phenotypes
  • Fanconi Anemia
Tags
Red Red List (low evidence)
NPM1
2 reviews
1 green 		Unknown
Sources
  • Expert list
  • Expert Review Red
Phenotypes
  • radial ray defects
  • short stature
  • nail dsytrophy
  • bone marrow failure
Tags
Red Red List (low evidence)
PITX1
4 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Other
Phenotypes
  • Liebenberg syndrome
  • Radially deviated wrists
Tags
Red Red List (low evidence)
PUF60
2 reviews
1 green 		MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Red
Phenotypes
  • Verheij syndrome, 615583
Tags
Red Red List (low evidence)
SAMD9
1 review
1 red 		MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Other
Phenotypes
  • MIRAGE syndrome 617053
Tags

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