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Congenital hypotrichosis diagnosis

CDH3-Related Congenital Hypotrichosis With Juvenile

Hypotrichosis simplex Genetic and Rare Diseases

  1. Hypotrichosis simplex is a rare form of hereditary hair loss without other abnormalities. Affected individuals typically show normal hair at birth, but experience hair loss and thinning of the hair shaft that starts during early childhood and progresses with age
  2. A wide range of conditions can present with congenital hypotrichoses/atrichia. Awareness of these conditions can help in the proper and timely diagnosis and counseling of affected families, and in some cases avoid unnecessary investigations
  3. Congenital Atrichia Hypotrichosis is the term dermatologists use to describe a condition of no hair growth. Unlike alopecia, which describes hair loss where formerly there was hair growth,..
  4. A wide range of conditions can present with congenital hypotrichoses/atrichia. counseling of affected families, and in some cases avoid unnecessary investigations. The rapid growth in genetic analysis of diseases has also led to an increased knowledge of the genetic and molecular basis of many of thes

Congenital Hypotrichosis and Congenital Atrichi

  1. Congenital means present at birth that usually describes a condition or abnormality. Other disorders that may be congenital are down syndrome, club foot, and Edwards syndrome. Hypotrichosis is a genetic condition in which a person experiences little to no hair growth. This condition will usually stay with the person throughout their lives
  2. Hypotrichosis, congenital, with juvenile macular dystrophy; HJMD; Juvenile macular dystrophy and congenital hypotrichosis. Symptoms Symptoms Listen. This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed
  3. The parents were counselled and a diagnosis of congenital hypotrichosis simplex (CHS) was made after extensive work up and investigations, ruling out metabolic and systemic disorders. Isolated variant of CHS is a rare disorder though hereditary hypotrichosis is uncommonly reported in literature [1]
  4. Congenital Hypotrichosis Congenital hypotrichosis is that hypotrichosis which is present at the time of birth. It is a very rare inherited disorder associated with the reduction of hair from birth and the development of countless milia that gradually disappears by adolescence. These milia may occur on face, armpits, chest and genital area
  5. alis: This is the characteristic werewolf syndrome form of the condition where a person experiences abnormal—and often stark—hair growth over large areas of their body. As opposed to lanugo, the hair is typically dark and may be quite thick

Congenital Hypotrichosis: Congenital Aplasia, Triangular

Congenital non-color-linked hair loss +/- additional ectodermal defects. Genetic coding for hypotrichosis (Birman and Siamese) → hair follicles and adnexa (sebaceous glands, sweat glands and arrector pili muscles) absent or hypoplastic and decreased in number → hairless or thin coat from birth Autosomal recessive hypotrichosis is a condition that affects hair growth. People with this condition have sparse hair (hypotrichosis) on the scalp beginning in infancy. This hair is usually coarse, dry, and tightly curled (often described as woolly hair). Scalp hair may also be lighter in color than expected and is fragile and easily broken

Congenital Hypotrichosis and Congenital Atrichia

Congenital Hypotrichosis No More Thin Edge

Congenital atrichia and hypotrichosis Congenital atrichia and hypotrichosis Antoni Bennàssar, Juan Ferrando, Ramon Grimalt Barcelona, Spain Background: Alopecia present from birth includes a proposed the first known classification based on broad differential diagnosis and often represents a diagnostic embryological principles This condition can be congenital or caused by disease. For the sake of this article, we'll focus on eyelash hypotrichosis. Medical Definition. Hypotrichosis, defined, is a medical term used to describe a condition in which natural hair growth does not occur Hypotrichosis with Juvenile Macular Dystrophy. Congenital hypotrichosis associated with juvenile macular dystrophy (MIM 601553) is a rare autosomal recessive disorder characterized by early hair loss, heralding progressive degeneration of the retinal macula leading to early blindness during the second to third decade of life [23, 24].HJMD prevalence is unknown and has only been reported in. Cambiaghi S, Barbareschi M. A sporadic case of congenital hypotrichosis simplex of the scalp: difficulties in diagnosis and classification. Pediatr Dermatol. 1999;16:301-304. Baumer A, Belli S, Trueb RM, et al. An autosomal dominant form of hereditary hypotrichosis simple maps to 18p11.32-p11.23 in an Italian family. Eur J Hum Genet. 2000;8:443.

Other genodermatoses with papular lesions and hypotrichosis: Oral-facial-digital syndrome - An X-linked dominant ectodermal dysplastic syndrome with congenital papular lesions and hypotrichosis. Patients also present with cleft lip / palate, hypoplastic alae nasi, brachydactyly, and intellectual disability and are at risk for polycystic. Hypotrichosis Hypotrichosis is a condition of abnormal hair patterns, predominantly loss or reduction. It occurs, most frequently, by the growth of vellus hair in areas of the body that normally produce terminal hair Birman Hypotrichosis and Short Life Expectancy (CHSLE) is an autosomal recessive syndrome described in the Birman cat breed (Felis silvestris catus). Hypotrichosis is a condition of abnormal hair growth, mainly hair loss or reduction. It is a characteristic of three domestic cat breeds, Sphynx, and cats related from Donskoy and Peterbald breed Entry H00785 Disease Name Congenital hypotrichosis with juvenile macular dystrophy Description Hypotrichosis with juvenile macular dystrophy is a rare autosomal recessive disorder characterized by sparse scalp hair from birth and resulting hair loss associated. HJMD has been described as macular degeneration and short sparse scalp hair from birth with hair loss during the first months of life.

Juvenile macular degeneration and hypotrichosis Genetic

(s): - Hypotrichosis, Marie Unna type - MUHH - Marie Unna congenital hypotrichosis Classification (Orphanet): - Rare genetic disease - Rare skin disease Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities - Epidemiological [csbg.cnb.csic.es] Summary Epidemiology Prevalence and incidence are unknown. Congenital hypotrichosis is suspected when a dog has areas of hair loss (that do not worsen) from birth or shortly thereafter. The diagnosis is confirmed through a skin biopsy, a simple procedure done with local anesthetic in which your veterinarian removes a small sample of your dog's skin for examination by a veterinary pathologist

Congenital Hypotrichosis. Hypotrichosis is the medical term used to describe a form of balding where -instead of hair loss - hair has never grown in that certain area. People who suffer from this condition are actually born with it. Therefore, they will not grow hair in those specific areas for their entire lives

Congenital Hypotrichosis Simplex - JPM

Non Technical Summary In U.S. Hereford cattle, hypotrichosis is a non-lethal defect with a simple autosomal recessive mode of inheritance which is often referred to in the literature as viable hypotrichosis, congenital hypotrichosis, or semi-hairless. In afflicted Herefords, the hair coat can be very short, fine, kinky, curly, or appear frosted and the tail switch can be underdeveloped

In this article the clinical and scanning electron microscopy findings of a nonfamilial case of congenital scalp hypotrichosis simplex are reported. In some patients the diagnosis of sporadic hypotrichosis simplex of the scalp should be considered after ruling out all other possible causes of congenital and hereditary hypotrichosis When a genetic skin disease issuspected, biopsy specimens of typically affected areas shouldbe submitted for diagnosis. References 1. L. Ackerman, Inheritance of baldy calf syndrome Mod Vet Pract 64: (1983) 807-2. J. Ayers, H. Leipold, R. Schalles, Pathologic studies of cross-related congenital hypotrichosis in cattle J Vet Med 36: (1989) 447-3. J

Medicine by Sfakianakis G

Congenital hypotrichosis is defined as a less than normal amount of hair, obvious at birth or in the first weeks of life. Causes are nongenetic or genetic. Objectives. To describe the clinical presentation and histological features of a novel form of hypotrichosis in a heifer. Anima Hypotrichosis. Hypotrichosis implies a less-than-normal amount of hair and a congenital, possibly hereditary, basis for the condition. 5, 16 Hypotrichosis may be regional or multifocal in distribution, but is usually generalized. Reports of hypotrichosis in the horse are extremely rare, anecdotal, and sketchy The rapid growth in genetic analysis of diseases has also led to an increased knowledge of the genetic and molecular basis of many of these conditions. This contribution briefly reviews updates on some of the most common conditions associated with congenital hypotrichosis/atrichia Congenital hypotrichosis with juvenile macular dystrophy (HJMD) is a rare autosomal recessive syndrome first reported by Wagner in 1935. Characteristic features comprise hair loss and progressive macular degeneration leading to reduced visual acuity and early blindness. EEM (ectodermal dysplasia, ectrodactyly and macular dystrophy) syndrome is a similar condition and is associated with.

Search for: Rare Disease Profiles; 5 Facts; Rare IQ; Rare Mystery; Diagnosis Congenital hypotrichosis is confirmed from the presenting history and signs, and by histopathological examination of skin biopsy samples which demonstrate low numbers or an absence of hair follicles, sebaceous glands, sweat glands and arrector pili muscles

Hypotrichosis - Definition, Causes and Treatmen

Hypotrichosis. Summary: Congenital lack of hair growth. 1, 2 More on Hypotrichosis » Causes List: Hypotrichosis. Some of the causes of the condition may include: 3 Causes of Hypotrichosis: 19q13.11 Microdeletion Syndrom Definition. A disorder characterized by congenital hypotrichosis, early hair loss, and severe degenerative changes of the retinal macula that culminate in blindness during the second to third decade of life Find details on Congenital hypotrichosis and alopecia in cats including diagnosis and symptoms, pathogenesis, prevention, treatment, prognosis and more. All information is peer reviewed Hypotrichosis: A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body. 2 • • • Hypotrichosis : Presence of less than the normal amount of hair Congenital hypotrichosis may be associated with other features, including epilepsy, chromosomal abnormalities, inborn errors of metabolism, and ocular, ectodermal, or skeletal abnormalities. If any associations are identified, workup for a syndromic cause should be performed and genetic counseling may be appropriate depending on the diagnosis.

Rat tail syndrome, a congenital form of hypotrichosis in cattle, is controlled by genes at two interacting loci. Because animals heterozygous for undesirable or lethal recessive traits often cannot be detected by visual examination, and sometimes exhibit a phenotype that is thought to be desirable, inadvertent selection may help spread genetic. Description Congenital hypothyroidism (CH) is inadequate thyroid hormone production in newborn infants. At one time referred to by now unacceptable term cretinism, congenital hypothyroidism is associated with either the congenital absence of a thyroid gland or the inability of the thyroid gland to secrete thyroid hormone. It can occur because of an anatomic defect in the gland, an inborn. HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD description, symptoms and related genes. Get the complete information in our medical search engine for phenotype-genotype relationship

Episodic weakness of Burmese cats. Nemaline myopathy. Myasthenia gravis. Duchenne muscular dystrophy. Myotonia congenita. Primary hyperoxaluria. Devon rex hereditary myopathy. Glycogen storage diseases. Amyloidosis - systemic amyloid accumulation in Abyssinian, Siamese and Oriental shorthair cats In addition, Chen and Liu (2017) reported a Chinese boy with an intermediate phenotype, showing both congenital cataract and hypotrichosis, who was compound heterozygous for missense mutations in the LSS gene: I342S (600909.0003) in the N-terminal domain and W629C (600909.0004) in the C-terminal domain

Hypertrichosis: Symptoms, Causes, Diagnosis, Treatment

Other findings in sheep include an absence of fibers in follicles, keratotic follicles, hypertrophy and hyperplasia of sebaceous glands and epidermis, and epidermal hyperkeratosis (Mackie and McIntyre, 1992).This white-tailed deer fawn represents the first case of congenital hypotrichosis observed in a cervid. Diagnosis as hypotrichosis was. Hypertrichosis is a condition that causes excessive hair growth all over the body, it is sometimes referred to as werewolf syndrome. The primary symptom of hypertrichosis is the presence of hair. Congenital hypotrichosis and nearly complete anodontia were diagnosed in 2 male Holstein calves. Monogenic, X-linked recessive inheritance was suspected. Chromosomal Xq-deletions were not detected. Molecular genetic marker analysis based on microsatellites revealed an exclusive joint genomic region on the long arm of the X-chromosome. Putative location of the gene locus for congenital.. Congenital hypotrichosis with juvenile macular dystrophy (HJMD) is a rare genetic disorder that causes early-age hair loss and vision loss that begins in childhood and becomes worse with time (progressive). Affected individuals are either born without hair (congenital hypotrichosis) or lose it within the first few months of life DISCUSSION The clinical history and histopathological findings in this case are most consistent with a diagnosis of congenital hypotrichosis. The onset of hair loss early in life, with the development of persistent alopecia in an otherwise healthy animal, is similar to the delayed or tardive type of hypotrichosis reported in cattle

Hypotrichosis with juvenile macular dystrophy is an autosomal recessive hereditary disease. It is caused by a combination of mutations ( compound heterozygosity) in the CDH3 gene, which codes for Cadherin-3 (also known as P-Cadherin), a calcium-binding protein that is responsible for cellular adhesion in various tissues Follicular dysplasia is the congenital abnormality of the morphogenesis of hair follicles leading to changes in the quality and/or quantity of the hair shaft and resulting in hypotrichosis. 8,9,11 Congenital hypotrichosis has been widely reported in all domestic veterinary species, but is most common in calves Symptoms via clinical synopsis from OMIM: 57 Skin Nails Hair Hair: hypotrichosis Skeletal Pelvis: coxa vara flared iliac wings short femoral neck limited hip abduction Head And Neck Teeth: normal teeth Chest Ribs Sternum Clavicles And Scapulae: medial [malacards.org] Showing of 18 Percent of people who have these symptoms is not available through HPO Autosomal dominant inheritance 0000006 Coxa.

Congenital Hypotrichosis - American Hair Loss Associatio

  1. Congenital insensitivity to pain with anhidrosis (CIPA) has two characteristic features: the inability to feel pain and temperature, and decreased or absent sweating (anhidrosis). This condition is also known as hereditary sensory and autonomic neuropathy type IV. The signs and symptoms of CIPA appear early, usually at birth or during infancy, but with careful medical attention, affected.
  2. These hypotrichosis disorders coexist with many other physical or mental problems. Disorders like Graham-Little syndrome, Hallermann-Streiff syndrome, Ofuji syndrome, congenital aplasia, alopecia triangularis, papular atrichia, metaphyseal chondrodysplasia, EEM Syndrome and cartilage-hair hypoplasia, manifest with the symptoms of hypotrichosis
  3. In 2 unrelated consanguineous families with congenital erythroderma with palmoplantar keratoderma, hypotrichosis, and hyper-IgE features suggestive of Netherton syndrome (NTS; 256500), Samuelov et al. (2013) excluded pathogenic mutations in the SPINK5 gene ().Whole-exome sequencing revealed 2 different homozygous mutations in the DSG1 gene (125670.0008 and 125670.0009) that segregated with.
  4. Q84.0 is a billable diagnosis code used to specify a medical diagnosis of congenital alopecia. The code Q84.0 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions. The ICD-10-CM code Q84.0 might also be used to specify conditions or terms like abnormal.

Tricho-retino-dento-digital syndrome is an autosomal dominant ectodermal dysplasia syndrome, characterized by uncombable hair syndrome (see this term), congenital hypotrichosis and dental abnormalities such as oligodontia (see this term) or hyperdontia, and associated with early-onset cataract, retinal pigmentary dystrophy, and brachydactyly. The initial testing for Alopecia, Congenital can begin with facial genetic analysis screening, through the FDNA Telehealth telegenetics platform, which can identify the key markers of the syndrome and outline the type of genetic testing needed. A consultation with a genetic counselor and then a geneticist will follow An autosomal recessive syndrome characterized by congenital hypotrichosis and short life expectancy has been described in the Birman cat breed (Felis silvestris catus). We hypothesized that a FOXN1 (forkhead box N1) loss-of-function allele, associated with the nude phenotype in humans, mice and rats, may account for the syndrome observed in Birman cats

Hypotrichosis - an overview ScienceDirect Topic

Dive into the research topics of 'Microscopic and ultrastructural study of the hair shaft: Significance and limits in diagnosis and of congenital hypotrichosis classification'. Together they form a unique fingerprint. Hypotrichosis Medicine & Life Sciences 100%. View full fingerprint. Congenital Alopecia/Hypotrichosis meaning the absence of hair or less hair than normal present a birth. Hereditary Alopecia/Hypotrichosis meaning the absence of hair or less hair than normal that is passed along from one's ancestry. Alopecia areata meaning hair occurring in circumscribed patches or places. Clinical Sign Congenital vertebral anomalies include alterations of shape and number of vertebrae. Coccygeal dysgenesis disorder is associated with varying degrees of agenesis/ aplasia of coccygeal vertebra. The 'rat-tail' syndrome (RTS) is a bovine congenital, inherited hypotrichosis characterized by misshaped, curly sparse hair and by missing hairs at the.

Total Hypotrichosis, Mari type is a rare congenital disorder, first described in the aboriginal Mari population in Russia. Both males and females may be affected. Worldwide, individuals of all racial and ethnic groups may be affected Marked hypotrichosis, Hypotrichosis, infantile, Congenital hypotrichosis [more] Congenital lack of hair growth. Hyperhidrosis: Profuse sweating, Always check with a qualified professional for healthcare information, treatment advice and/or diagnosis Q80.9 is a billable diagnosis code used to specify a medical diagnosis of congenital ichthyosis, unspecified. The code Q80.9 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions. The ICD-10-CM code Q80.9 might also be used to specify conditions or terms like. Congenital disorders of keratinization characterized by noninflammatory dryness and scaling of the skin, often associated with other defects and with abnormalities of lipid metabolism; distinguishable genetically, clinically, microscopically, and by epidermal cell kinetics. Synonym (s): alligator skin, fish skin, sauriasis Juvenile macular dystrophy and congenital hypotrichosis; Overview. No overview is available at this time. Please check back for future updates. For more information, medical advice of their qualified health care professionals before seeking any information related to their particular diagnosis, cure or treatment of a condition or disorder..

Bovine hypotrichosis is a congenital disease characterized by partial or complete absence of hair coat, with or without accompanying developmental defects (Jayasekara et al., 1979). At least six different forms of congenital hypotrichosis are distinguished including lethal (semi-lethal), partialisvitalis (viable), areata, semi-hairlessness Submit your diagnosis to see full explanation. and hypotrichosis, These abnormal facies may be mistaken for the manifestations of congenital syphilis. 2,3 Wrinkled or hyperpigmented skin. Causes and symptoms. Hypotrichosis may be congenital and acquired. The reason for the first state is genetic heredity. But there are many different acquired causes of eyelash loss. They are: allergy to mascaraThe loss cause may be a reaction to mascara, including allergic. Allergies can be caused by chemicals in the mascara Hereditary hypotrichosis simplex of the scalp is a genotrichosis characterized by sparse or absent scalp hair without structural defects, in the absence of other ectodermal or systemic abnormalities. We describe two Spanish families with hypotrichosis of the scalp. We believe these families have Toribio and Quiñones type hereditary hypotrichosis simplex of the scalp

From my description of Kyle, plus the photos I sent, the vet at Penn State agreed that congenital hypotrichosis was a very likely diagnosis. He did say that if Kyle's dam had a high fever during the phase of follicle development (she didn't though) it could result in a loss of hair in the fetus (see fetal timeline below) Congenital insensitivity to pain (CIP) is an extremely rare inherited condition that inhibits the ability to perceive physical pain. From birth, affected individuals never feel pain in any part of their body when injured 1). Individuals with congenital insensitivity to pain do not feel pain from any noxious stimuli, including inflammation and.

Congenital Hypotrichosis in Dogs - Symptoms, Causes

  1. ation, skin biopsies, skull radiographs, and DNA analysis of a 2-day-old Red Angus-Charolais-Simmental cross bull calf confirmed the diagnosis of congenital hypotrichosis and anodontia defect (HAD), also called anhidrotic ectodermal dysplasia, which is a rare anomaly caused by a deletion in the bovine EDA gene on the X chromosome
  2. Patients with congenital hypertrichosis lanuginosa have growth of the lanugo hair, which increases in length and extent of involvement from birth to approximately age 2 years (range, 1-8 y). As a result, the density, length, and extent of involvement may decrease; the rate of hair growth also slows
  3. The code Q80.9 is VALID for claim submission. Code Classification: Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) Other congenital malformations (Q80-Q89) Congenital ichthyosis (Q80) Q80.9 Congenital ichthyosis, unspecified. Code Version: 2020 ICD-10-CM
  4. Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare genetic disease that clinicians are unlikely to have encountered. Patients usually initially present with sparse scalp hair (congenital hypotrichosis) from birth HJMD is a rare genetic disease that clinicians are unlikely to have encountered
  5. Congenital cataract - most commonly bilateral; can be focal or complete; Differential diagnosis. Hutchinson-Gilford progeria syndrome (HGPS) HGPS is a rare genetic syndrome that is classically associated with progressive premature aging and particular facial features such as a small face, micrognathia, and a thin, pointed nose with hypotrichosis
  6. diagnosis. It is also important to inspect the hair shaft with a magnifying glass. A hair with a clean break is the result of excessive rabbits with congenital hairlessness or hypotrichosis. In order not to spread this mutation among the offspring, these rabbits should be removed from breeding lines. They can
  7. Hypotrichosis. Hypotrichosis comes to us from 'hypo-', which denotes a deficient amount of something,'-trich-', which refers to hair and '-osis', which refers to an abnormal condition of some sort.

The symptoms of Hypertrichosis mainly include excessive hair growth. The condition affects members of either sex. A fine layer of hair called Lanugo normally covers the fetus and falls of sometime before the fetus comes out of the womb. In case of Congenital Hypertrichosis sufferers, the Lanugo continues to grow Symptoms of the disease with congenital hypotrichosis are a partial or complete absence of eyelashes, eyebrows and hair on the head from the moment of birth. Such a disease is quite rare, is equally found in both sexes and is not treatable. Acquired pathology is the consequence of any problem affecting the hair follicles or the structure of the. Congenital Defects of the Gastrointestinal (GI) System include: * Atresia or blockages of various areas along the intestinal tract. This condition is uncommon in foals and it is not related to the Lethal White Disease. The segment of intestines most often involved is the colon (atresia coli), although it has also been described in the rectum.

A type 1 excludes note is a pure excludes. It means not coded here. A type 1 excludes note indicates that the code excluded should never be used at the same time as Q84.1.A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition Hair loss in children and adolescents can result from various conditions, which may be acquired or congenital and range in severity. Hair loss can present in otherwise healthy patients, or it can be a sign of underlying malnutrition, toxicity, or systemic disease. Tinea capitis (TC), telogen effluvium (TE), traction alopecia (TA. Hypertrichosis, also known as werewolf syndrome, is a condition characterized by excessive hair growth anywhere on a person's body. It can affect both women and men, but it's extremely rare.

Acquired Hypertrichosis - this happens after birth.; Congenital hypertrichosis - this is because of a defect that has been present since they were born or as a result of a congenital defect and is a rare class. It is so rare that there have only been fifty cases verified. Hypertrichosis Symptoms. The main symptom of hypertrichosis is hair growth that is excessive A syndrome characterized by severe dermatitis, multiple allergies and metabolic wasting. Clinical features include erythroderma, yellowish papules and plaques arranged at the periphery of the palms, along the fingers and over weight-bearing areas of the feet, skin erosions and scaling, and hypotrichosis

Congenital immunodeficiency is present at the time of birth, and is the result of genetic defects. These immunodeficiency disorders are also called primary immunodeficiencies. Even though more than 70 different types of congenital immunodeficiency disorders have been identified, they rarely occur BDCS should be considered as a differential diagnosis in patients with early onset or familial basal cell carcinomas. A Scottish family with Bazex-Dupré-Christol syndrome: follicular atrophoderma, congenital hypotrichosis, and basal cell carcinoma. | Journal of Medical Genetic Congenital hypotrichosis in a French bulldog Congenital hypotrichosis in a French bulldog Marks, A.; Broek, A. H. M.; Else, R. W. 1992-09-01 00:00:00 J I INTRODUCTION Congenital alopecia is defined as a partial or total absence of hair manifest at birth and due to developmental factors (Ebling and others 1986). It is occasionally accompanied by further ectodermal defects such as absence of. ICD-9-CM 374.55 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 374.55 should only be used for claims with a date of service on or before September 30, 2015