AREDYLD syndrome
|
(Orphanet:1133)
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Ablepharon macrostomia syndrome
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(Orphanet:920)
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Bartsocas-Papas syndrome
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(Orphanet:1234)
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CARDIOFACIOCUTANEOUS SYNDROME 2
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(OMIM:615278)
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CARDIOFACIOCUTANEOUS SYNDROME 4
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(OMIM:615280)
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Cardiofaciocutaneous syndrome
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(Orphanet:1340)
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ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE
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(OMIM:602032)
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Fraser syndrome
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(Orphanet:2052)
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Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome
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(Orphanet:306542)
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Glomerulonephritis - sparse hair - telangiectasis
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(Orphanet:2087)
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Hidrotic ectodermal dysplasia, Christianson-Fourie type
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(Orphanet:1808)
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Hypotrichosis - lymphedema - telangiectasia
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(Orphanet:69735)
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Ichthyosis follicularis - alopecia - photophobia
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(Orphanet:2273)
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Keratosis follicularis - dwarfism - cerebral atrophy
|
(Orphanet:2339)
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Neuroectodermal syndrome, Johnson type
|
(Orphanet:2316)
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PARC syndrome
|
(Orphanet:2825)
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Pseudoprogeria syndrome
|
(Orphanet:2985)
|
Pure hair and nail ectodermal dysplasia
|
(Orphanet:69084)
|
Spastic paraplegia - neuropathy - poikiloderma
|
(Orphanet:2821)
|
Tricho-oculo-dermo-vertebral syndrome
|
(Orphanet:3354)
|
X-linked hypohidrotic ectodermal dysplasia
|
(Orphanet:181)
|