Spondyloepimetaphyseal Dysplasia with Hypotrichosis - Ontology Browser

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Spondyloepimetaphyseal Dysplasia with Hypotrichosis (DOID:9001447)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)

Parent Terms

Term With Siblings

Child Terms

hypotrichosis + is-a

spondyloepimetaphyseal dysplasia + is-a

alopecia +

anauxetic dysplasia 1

Anauxetic Dysplasia 2

autosomal recessive congenital ichthyosis 11

autosomal recessive woolly hair 3

Basaran Yilmaz Syndrome

Bazex-Dupre-Christol Syndrome

Brachymetapody-Anodontia-Hypotrichosis-Albinoidism

Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE

congenital hypotrichosis with juvenile macular dystrophy

Dyggve-Melchior-Clausen disease +

Ectodermal Dysplasia, Trichoodontoonychial Type

hypohidrotic ectodermal dysplasia +

hypotrichosis 1

hypotrichosis 10

hypotrichosis 11

hypotrichosis 12

hypotrichosis 13

hypotrichosis 14

hypotrichosis 2

hypotrichosis 3

hypotrichosis 4

hypotrichosis 5

hypotrichosis 6

hypotrichosis 7

hypotrichosis 8

hypotrichosis 9

hypotrichosis and recurrent skin vesicles

hypotrichosis of eyelid

Hypotrichosis, Progressive Patterned Scalp, with Wiry Hair, Onycholysis, and Cleft Lip/Palate

hypotrichosis-lymphedema-telangiectasia syndrome +

Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome

Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis

Loucks-Innes Syndrome

metatropic dysplasia

Nicolaides Baraitser Syndrome

Rombo syndrome

Schimke immuno-osseous dysplasia

Schopf-Schulz-Passarge syndrome

Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis

Spondyloepimetaphyseal Dysplasia with Abnormal Dentition

Spondyloepimetaphyseal Dysplasia with Hypotrichosis

Spondyloepimetaphyseal Dysplasia with Joint Laxity +

SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE

Spondyloepimetaphyseal Dysplasia, Faden-Alkuraya Type

spondyloepimetaphyseal dysplasia, Genevieve-type

Spondyloepimetaphyseal Dysplasia, Irapa Type

Spondyloepimetaphyseal Dysplasia, Isidor-Toutain Type

Spondyloepimetaphyseal Dysplasia, Krakow Type

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related

spondyloepimetaphyseal dysplasia, Missouri type

spondyloepimetaphyseal dysplasia, Pakistani type

Spondyloepimetaphyseal Dysplasia, Shohat Type

spondyloepimetaphyseal dysplasia, Sponastrime type

spondyloepimetaphyseal dysplasia, Strudwick type

Spondyloepimetaphyseal Dysplasia, X-Linked

spondyloepiphyseal dysplasia congenita

spondyloepiphyseal dysplasia tarda +

spondyloepiphyseal dysplasia with congenital joint dislocations

Storm Syndrome

Trichoodontoonychial Dysplasia

X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy

Synonyms
Exact Synonyms:	Whyte Petersen McAlister syndrome ; Whyte syndrome
Primary IDs:	MESH:C535783
Alternate IDs:	RDO:0001087

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.

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