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• List of Sites

• ICHTHYOSIS--CHEEK--EYEBROW SYNDROME
• Ichthyosis cheek eyebrow syndrome

• See Centromeric Instability Immunodeficiency Syndrome

• List of Sites
• -Alopecia-Eclabion-Ectropion-Mental Retardation Syndrome
• ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION
• -Camptodactyly Syndrome
• See Camptodactyly-Ichthyosis Syndrome
• -Cheek-Eyebrow Syndrome
• See ICE Syndrome
• -Hepatosplenomegaly-Cerebellar Degeneration Syndrome
• ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION
• -Spastic Neurologic Disorder-Oligophrenia Syndrome
• See Sjogren-Larsson Syndrome
• with Large Keratohyalin Granules in the Skin
• ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN
• Erythroderma
• -Corneal Involvement-Deafness Syndrome
• See KID Syndrome
• Congenital (Brocq)
• Also see Netherton Syndrome
• Bullous Form (Epidermolytic Hyperkeratosis)
• Bullous ichtyosiform erythroderma congenita
• BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQ
• Nonbullous Form
• Type 1 (Nonbullous Congenital Ichthyosiform Erythroderma, Type I)
• ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS, 1
• Follicularis
• -Atrichia-Photophobia Syndrome
• See IFAP Syndrome
• Hystrix-Like
• with Deafness (HID Syndrome)
• ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
• with Oral and Digital Anomalies
• ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS

• See Gilbert's Syndrome

• DIABETES MELLITUS, CONGENITAL INSULIN-DEPENDENT, WITH FATAL SECRETORY DIARRHEA

• See Celiac Disease/Sprue

• ICHTHYOSIS FOLLICULARIS, ATRICHIA, AND PHOTOPHOBIA SYNDROME

• DEFICIT SELETTIVO DI IgA 

• See Twins, Conjoined, Pygopagus

• Arthrogryposis multiplex congenita cns calcifications
• Arthrogryposis multiplex congenita whistling face
• ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE

• Craniosynostosis radial aplasia type imaizumi

• IMMOTILE CILIA SYNDROME 1; ICS1

• 5
• See Duncan Disease
• 6/Wiskott Aldrich Type
• See Wiskot Aldrich Syndrome

• X-Linked
• See Woods Black Norbury Syndrome

• Anorectal anomalies
• ANORECTAL ANOMALIES

• Chondrodysplasia situs inversus imperforate anus polydactyly

• List of Sites

• See Lateral Incisors, Pegged or Missing/Absent

• Familial
• Type I
• See Reifenstein Syndrome
• Type II
• See Pseudovaginal Perineoscrotal Hypospadias

• List of Sites

• INDIFFERENCE TO PAIN
• CONGENITAL ANALGESIA

• See Caffey Disease

• List of Sites

• Intersex Society of North America
• Related Books

• Chronic
• Chronic Intestinal Pseudo-Obstruction
• Intestinal Pseudo-Obstruction
• Links to related web pages

• List of Sites

• IDEAS (Inverted Duplication Exchange, Advocacy and Support)
• chromosome 15 inverted duplication
• FACTS ABOUT ISODICENTRIC 15
• Support Group

• See Urofacial syndrome

• See Spondyloepiphyseal Dysplasia/Dystosis

• Type I/Autosomal Dominant
• IRIDOGONIODYSGENESIS, TYPE 1; IRID1
• Type II (Iridogoniodysgenesis Syndrome; Iris Hypoplasia with Early-Onset Glaucoma, Autosomal Dominant)
• IRIDOGONIODYSGENESIS, TYPE 2; IRID2
• with Somatic Anomalies
• See Rieger Syndrome

• with Glaucoma
• IRIS, HYPOPLASIA OF, WITH GLAUCOMA; IHG
• Autosomal Dominant
• See Iridogoniodysgenesis, Type II

• Hereditary
• See Anemia, Hereditary Sideroblastic

• Isaacs' Syndrome
• Continuous muscle fiber activity hereditary
• CONTINUOUS MUSCLE FIBER ACTIVITY, HEREDITARY

• See Twins, Conjoined, Ischopagus

• See Inverted Duplication 15

• See Microtia-Aortic Arch Syndrome

• List of Sites

• See Incontinentia Pigmenti Achromians

• ASPLENIA WITH CARDIOVASCULAR ANOMALIES

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